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EP1626967A1 - Substituted pyrazoles - Google Patents

Substituted pyrazoles

Info

Publication number
EP1626967A1
EP1626967A1 EP04718277A EP04718277A EP1626967A1 EP 1626967 A1 EP1626967 A1 EP 1626967A1 EP 04718277 A EP04718277 A EP 04718277A EP 04718277 A EP04718277 A EP 04718277A EP 1626967 A1 EP1626967 A1 EP 1626967A1
Authority
EP
European Patent Office
Prior art keywords
pyrazol
phenyl
ylmethyl
biphenyl
fluoro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04718277A
Other languages
German (de)
French (fr)
Inventor
Kai Schiemann
Karl-August Ackermann
Michael Arlt
Dirk Finsinger
Oliver Schadt
Christoph Van Amsterdam
Gerd Bartoszyk
Christoph Seyfried
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Patent GmbH
Original Assignee
Merck Patent GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Publication of EP1626967A1 publication Critical patent/EP1626967A1/en
Withdrawn legal-status Critical Current

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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D491/08—Bridged systems

Definitions

  • the invention relates to the use of the compounds of the formula
  • R 2 (CH 2 ) n Het, (CH 2 ) n Ar, cycloalkyl with 3 to 7 C atoms or CF 3l
  • R 5 H or A A unsubstituted or substituted by shark or CN straight-chain or branched alkyl or cycloalkyl having 2 to 4 carbon atoms, having 1 to 10 carbon atoms, alkenyl having 2 to 10 carbon atoms, alkoxyalkyl having 2 to 10 carbon atoms or cycloalkyl 4 to 7 carbon atoms,
  • Het an organic radical containing heteroatoms in particular an unsubstituted or mono- or polysubstituted by A and / or shark, saturated, unsaturated or aromatic mono- or bicyclic heterocyclic or a linear radical containing one or two heteroatoms and having 1 to 15 carbon atoms,
  • Ar is an aromatic organic radical, in particular an unsubstituted or singly or multiply by A and / or
  • n 0, 1, 2, 3, 4 or 5
  • the object of the invention was to find compounds which can be used for the production of medicaments. It has been found that the compounds of the formula I and their salts and solvates have very valuable pharmacological properties with good tolerability.
  • the invention relates in particular to the compounds mentioned in the examples, which have the properties and properties which are described in the present application
  • the compounds of the formula I according to the invention are particularly suitable as ligands of 5 HT receptors, in particular of 5 HT2A and / or 5HT2C receptors, and can be used in human and veterinary medicine for the prophylaxis and treatment of various diseases of the central nervous system, such as e.g. Schizophrenia, Depression, Dementia, Parkinson's Disease, Alzheimer's Disease, Lewy Bodies Dementia, Huntington's, Tourette's Syndrome, Anxiety, Learning and
  • the compounds of the formula I and / or their physiologically acceptable salts or solvates are particularly preferred for the preparation of a medicament for the prophylaxis and / or treatment of psychoses, neurological disorders, amyotrophic lateral skierosis, eating disorders such as bulimia, nervous anorexia, premenstrual syndrome and / or positive influence on obsessive-compulsive disorder (OCD).
  • psychoses neurological disorders, amyotrophic lateral skierosis, eating disorders such as bulimia, nervous anorexia, premenstrual syndrome and / or positive influence on obsessive-compulsive disorder (OCD).
  • OCD obsessive-compulsive disorder
  • the compounds have a central nervous system.
  • the compounds have a strong affinity for 5-HT 2A receptors, furthermore they show 5-HT 2A receptor antagonistic properties.
  • test can be used, for example, for in-vitro detection of the affinity for 5-HT 2A receptors.
  • the ⁇ -HT ⁇ Receptors are exposed to both [ 3 H] ketanserin (a substance known for its affinity for the receptor) and the test compound.
  • the decrease in the affinity of [ 3 H] ketanserin for the receptor is an indication of the affinity of the test substances for the 5-HT 2 A receptor.
  • the proof is made analogously to the description by JE Leysen et al.,
  • the effectiveness of the compounds of the invention as 5-HT 2A receptor antagonists can be used in vitro analog W. Feniuk et al, Mechanisms of 5-hydroxytryptamine-induced vasoconstriction in. The Peripheral Actions of 5-Hydroxytryptamine, ed Fozard JR, Oxford. University Press, New York, 1989, p.110.
  • the contractility of the rat tail artery, caused by 5-hydroxytryptamine is mediated by 5-HT 2 A receptors.
  • vascular rings prepared from the ventral rat tail artery, are perfused in an organ bath with an oxygen-saturated solution. A response to the cumulative concentration of 5-HT is obtained by adding increasing concentrations of 5-hydroxytryptamine to the solution. Then the test compound in suitable concentrations in the
  • the 5-HT 2A antagonistic property can be determined in vivo analogously to MDSerdar et al., Psychopharmacology, 1996, 128: 198-205.
  • the compounds of the formula I are therefore suitable both in veterinary and in human medicine for the treatment of functional disorders of the central nervous system and of inflammation. They can be used for prophylaxis and for combating the consequences of cerebral infarction (apoplexia cerebri) such as stroke and cerebral ischemia, as well as for the treatment of extrapyramidal-motor side effects of neuroleptics and Parkinson's disease, for the acute and symptomatic therapy of Alzheimer's disease and for the treatment of amyotrophic lateral Sclerosis can be used. They are also suitable as therapeutic agents for the treatment of brain and spinal cord trauma.
  • OCD e.g. WO 9524194
  • anxiety and physiological changes associated with anxiety such as Tachycardia, tremor or sweating (e.g. EP 319962), panic attacks, psychoses, schizophrenia, anorexia, compulsive delusions, agoraphobia, migraines, Alzheimer's disease, sleep disorders as well as sleep apnea, tardive dyskinesias, learning disorders, age-related memory disorders, e.g. drug abuse disorders such as bulimia disorders alcohol, opiates, nicotine, psychostimulants such as Cocaine or amphetamines (e.g. US 6004980), sexual dysfunction, all types of pain and fibromyalgia (e.g. WO 9946245).
  • Tachycardia tremor or sweating
  • panic attacks e.g. EP 319962
  • psychoses schizophrenia, anorexia, compulsive delusions, agoraphobia, migraines, Alzheimer's disease, sleep disorders as well as sleep apnea,
  • EPS extrapyramidal side effects
  • EPS is characterized by Parkinson's-like syndromes, akathisia and dystonic reactions (e.g. EP 337136). They are also suitable for the treatment of nervous anorexia, angina,
  • Reynaud's phenomenon coronary vasospasm, in the prophylaxis of migraines (e.g. EP 208235), pain and neuralgia (e.g. EP 320983), for the treatment of Rett syndrome with autistic traits, Asperger's syndrome, autism and autistic disorders, in cases of poor concentration, Developmental disorders, hyperactivity states with mental underdevelopment and stereotypical behavioral states (eg WO 9524194).
  • endocrine diseases such as hyperprolactinaemia, also for vasospasm, thrombotic
  • the compounds according to the invention are further suitable for reducing the intraocular pressure and for glaucoma treatment. They are also suitable for the prophylaxis and treatment of poisoning symptoms when ergovalin is administered to animals.
  • the compounds are also suitable for the treatment of diseases of the cardiovascular system (WO 99/11641, page 3, lines 14-15).
  • the compounds according to the invention can also be used together with other active substances in the treatment of schizophrenia.
  • Other compounds which may be used are the compounds mentioned in WO 99/11641 on page 13, lines 20-26.
  • the compounds of formula I can be used as active pharmaceutical ingredients in human and veterinary medicine. They can also be used as intermediates for the production of further active pharmaceutical ingredients.
  • the invention accordingly relates to the use of the compounds of the formula I in human and veterinary medicine.
  • the compounds of formula I are preferably prepared by firstly preparing a compound of formula II
  • R 1 and X have the meanings given above, with a compound of the formula III
  • R 1 and X have the meanings given above, with a compound of the formula IV
  • the compounds of formula IA and IB can be obtained by using reducing agents such as e.g. Lithium aluminum hydride in the corresponding alcohols of the formulas IC and ID
  • the compounds of the formulas IE and IF can in turn be prepared using known nucleophiles, such as nitrogen bases, in particular hydroxylamine, O-methylhydroxylamine, morpholine, piperidine, piperain, N-ivlethylpiperazine, 4-methylpiperain-1-ylarnine, pyrrolidine, Pyrazolidine or Imida ⁇ olidin, optionally aminated in the presence of a reducing agent such as sodium triacetoxyborohydride or reacted to the corresponding imines.
  • nucleophiles such as nitrogen bases, in particular hydroxylamine, O-methylhydroxylamine, morpholine, piperidine, piperain, N-ivlethylpiperazine, 4-methylpiperain-1-ylarnine, pyrrolidine, Pyrazolidine or Imida ⁇ olidin, optionally aminated in the presence of a reducing agent such as sodium triacetoxyborohydride or reacted to the corresponding imines.
  • the compounds of the formulas IE and IF can be converted by Wittig reaction with methoxymethyltriphenylphosphonium salts to the corresponding enol ethers, which by treatment with an acid in the homologated aldehydes IG and IH
  • the compounds of the formulas IG and IH can be converted analogously to the compounds of the formulas IE and IF to the further compounds of the formula I.
  • Solvates of the compounds of the formula I are understood to mean the addition of inert solvent molecules to the compounds of the formula I, which are formed on account of their mutual attraction. Solvates are e.g. Mono- or dihydrates or alcoholates.
  • R 1 preferably represents A, shark, (CH 2 ) n Het or (CH 2 ) n Ar, in particular A, (CH 2 ) n Het or (CH 2 ) n Ar.
  • R 1 very particularly preferably denotes phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl-, ethyl-, n-propyl- or n-butylphenyl , 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5- or 3,6-difluoro-, dichloro- or dicyanophenyl, 3,4,5-trifluorophenyl , 3,4,5-
  • R 2 preferably denotes (CH 2 ) n Het, (CH 2 ) nNHA, (CH 2 ) nNHCH 2 Het or (CH 2 ) n Ar, in particular (CH 2 ) n Het, (CH 2 ) n NHA, (CH 2 ) n NHCH 2 Het.
  • R 2 very particularly preferably denotes phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl-, ethyl-, n-propyl- or n-butylphenyl , 2,3-, 2,4-, 2,5-, 2,6-difluoro- or dicyanophenyl, thiophene-2-yl or thiophene-3-yl, 2-, 3- or 4-pyridyl, 2-, 4- or 5-oxazolyl, 2-, 4- or 5-thiazolyl, quinolinyl, isoquinolinyl, 2- or 4-pyridazyl, 2-, 4- or 5-
  • R 4 particularly preferably denotes H.
  • R 5 preferably has the meaning A.
  • A is preferably alkyl, is preferably unbranched and has 1, 2, 3,
  • 4, 5, 6, 7, 8, 9 or 10 carbon atoms preferably 1, 2, 3, 4, 5 or 6 carbon atoms and preferably means methyl, ethyl, n- or propyl, further preferably isopropyl, butyl, isobutyl, sec-butyl or tert-butyl, but also n-pentyl, neopentyl, isopentyl or n-hexyl. Is particularly preferably methyl, ethyl, n-propyl, isopropyl 'pyl, n-butyl, n-pentyl, n-hexyl or n-decyl.
  • A also preferably has the meaning of the group (CH 2 ) m OCH 3 or (CH 2 ) m C 2 H 5 , where m is 2, 3, 4, 5 or 6, but in particular 2.
  • A is alkenyl, it is preferably allyl, 2- or 3-butenyl, isobutenyl, sec-butenyl, 4-pentenyl, iso-
  • Het is preferably an unsubstituted or aromatic and in particular saturated heterocyclic radical which is substituted by A.
  • Het preferably denotes 1-piperidyl, 1-piperazyl, 1- (4-methyl) -piperazyl, 4-
  • Het is particularly preferably one of the following radicals:
  • Ar preferably denotes an unsubstituted or by shark, OH, CN,
  • n is preferably 0, 1 or 2, in particular 0 or 1.
  • Cycloalkyl preferably has 3-7 C atoms and preferably represents cyclopropyl and cyclobutyl, further preferably cyclopentyl or cyclohexyl, furthermore also cycloheptyl, cyclopentyl is particularly preferred.
  • the compounds of the formula I have one or more chiral carbon atoms, the enantiomers, diastereomers and mixtures thereof are the subject of the present invention.
  • the invention relates in particular to those compounds of the formula I in which at least one of the radicals mentioned has one of the preferred meanings indicated above.
  • Some preferred groups of compounds can be expressed by the following partial formulas 11 to 19, which correspond to the formula I and in which the radicals which are not specified are those given in the formula I.
  • R 1 is (CH 2 ) n Het or (CH 2 ) ⁇ Ar;
  • R 2 is (CH 2 ) n Ar
  • R 1 is (CH 2 ) n Ar R 2 (CH 2 ) n Ar;
  • R 2 (CH 2 ) ⁇ Ar R 4 H R 3 (CHzJn-Het, (CH 2 ) n NHA, (CH 2 ) n NHCH 2 -Het, (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) n N (R 5 ) 2 or CH N-OA;
  • Hexyl or n-decyl n is 0, 1 or 2;
  • R 3 H R 4 (CH 2 ) nCO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) ⁇ -Het,
  • Hexyl or n-decyl n is 0, 1 or 2;
  • the compounds of the formula I and also the starting materials for their preparation are otherwise prepared by methods known per se, as described in the literature (for example in the standard works such as Houben-Weyl, methods of organic chemistry, Georg-Thieme-Verlag, Stuttgart) , are described, namely under reaction conditions which are known and suitable for the reactions mentioned. Use can also be made of variants which are known per se and are not mentioned here in detail.
  • the compound of formula III is preferably by reacting
  • R 2 and A have the meaning given above, obtained under conditions known for such reactions.
  • the starting materials can also be formed in situ, so that they are not isolated from the reaction mixture, but instead are immediately reacted further to give the compounds of the formula I.
  • the reactions of the compounds of the formula II with the compounds of the formula III and the compounds of the formula IV are carried out in the presence or absence of a preferably inert solvent at temperatures between about -20 and about 150 °, preferably between 20 and 100 °.
  • Suitable inert solvents are e.g. Hydrocarbons such as hexane, petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons such as trichlorethylene, 1, 2-dichloroethane, carbon tetrachloride, chloroform or
  • dichloromethane Alcohols such as methanol, ethanol, isopropanol, n-propanol, n-butanol or tert-butanol; Ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran (THF) or dioxane; Glycol ethers such as ethylene glycol monomethyl or monoethyl ether (methyl glycol or ethyl glycol), ethylene glycol dimethyl ether (diglyme); Ketones such as acetone or butanone; Amides such as acetamide, dimethylacetamide or dimethylformamide (DMF); Nitriles such as acetonitrile; Sulfoxides such as dimethyl sulfoxide (DMSO); Nitro compounds such as nitromethane or nitrobenzene; Esters such as ethyl acetate or mixtures of the solvents mentioned.
  • Alcohols such as methanol, ethanol, isoprop
  • the pH value required for the reaction can be adjusted on the basis of pH values selected for similar reactions of carbonyl with amino compounds.
  • the pH is preferably predetermined by the use of the respective acid addition salt, preferably a hydrogen halide addition salt of the compound of the formula II, ie there is no additional base or acid addition for reaction mix.
  • Preferred acid addition salts are hydrochlorides or bromides
  • a base of the formula I can be converted into the associated acid addition salt using an acid, for example by reacting equivalent amounts of the base and the acid in an inert solvent such as ethano! and then evaporating.
  • acids that provide physiologically acceptable salts are suitable for this implementation.
  • So inorganic acids can be used, e.g. Sulfuric acid, nitric acid, hydrohalic acids such as hydrochloric acid or hydrobromic acid, phosphoric acids such as orthophosphoric acid, sulfamic acid, also organic acids, especially aliphatic, alicyclic, araliphatic, aromatic or heterocyclic mono- or polybasic carboxylic, sulfonic or sulfuric acids, e.g. Formic acid, acetic acid, propionic acid, pivalic acid, diethyl acetic acid,
  • the free bases of formula I can be liberated from their salts with bases (e.g. sodium or potassium hydroxide or carbonate).
  • the preferred object of the invention is the use of the compounds of formula I and / or their physiologically acceptable
  • Salts and / or solvates for the production of pharmaceutical preparations, for the treatment or prophylaxis of diseases which can be influenced by the binding of the compounds of the formula I to 5 HT receptors, in particular in a non-chemical way. They can be used together with at least one solid, liquid and / or semi-liquid
  • Carrier or auxiliary and optionally in combination with an or several other active ingredients are brought into a suitable dosage form.
  • the invention further relates to pharmaceutical preparations containing at least one compound of the formula I and / or one of its physiologically acceptable salts and / or solvates for the treatment or prophylaxis of diseases which are influenced by the binding of the compounds of the formula I to 5 HT receptors ,
  • Suitable carriers are organic or inorganic substances which are suitable for enteral (e.g. oral), parenteral or topical application and do not react with the new compounds, for example water, vegetable oils, benzyl alcohols, alkylene glycols, polyethylene glycols, glycerol triacetate,
  • Gelatin carbohydrates such as lactose or starch, magnesium stearate, talc, petroleum jelly. Tablets, pills, dragees, capsules, powders, granules, syrups, juices or drops are used for oral use, suppositories for rectal use, solutions, preferably oily or aqueous solutions, and suspensions for parenteral use.
  • Emulsions or implants for topical application of ointments, creams or powders.
  • the new compounds can also be lyophilized and the lyophilizates obtained e.g. can be used for the production of injectables.
  • the specified preparations can be sterilized and / or contain auxiliaries such as lubricants, preservatives, stabilizers and / or wetting agents, emulsifiers, salts for influencing the osmotic pressure, buffer substances, coloring, flavoring and / or one or more further active ingredients, eg one or more vitamins.
  • the substances according to the invention are generally preferably administered in doses between 1 and 500 mg, in particular between 5 and 100 mg, per dosage unit.
  • the daily dosage is preferably between about 0.02 and 10 mg / kg body weight.
  • the specific dose for each patient depends on a wide variety of factors, for example on the effectiveness of the particular compound used, on age, body weight, in general Health status, gender, the diet, the time and route of administration, the rate of excretion, the combination of drugs and the severity of the disease to which the therapy applies. Oral application is preferred.
  • Preferred compounds of the formula I have nanomolar affinity for the 5 HT2A receptors, some with low affinity for the 5 HT2C receptor.
  • customary work-up means: if necessary, water is added, extracted with ethyl acetate or dichloromethane, the mixture is separated off, the organic phase is dried over sodium sulfate, evaporated and purified by chromatography on silica gel and / or by crystallization.
  • a solution of 2.090 g 9 in 25 ml THF is added dropwise to a suspension of 1.139 g lithium aluminum hydride in 25 ml tetrahydrofuran with stirring and ice cooling under a nitrogen atmosphere. After stirring for 1 h, a further 0.500 g of lithium aluminum hydride are added. After stirring for a further 2 h, saturated sodium chloride solution is added dropwise while cooling with ice and the mixture is worked up in the customary manner, giving 10.
  • Methyl hydroxylamine hydrochloride 23 in 8.50 ml dichloroethane and 4.5 ml tetrahydrofuran are added 0.033 ml acetic acid and stirred for 3 hours.
  • the mixture is stirred for 3 h and then 130.287 mg of sodium triacetoxyborohydride are added. After stirring for 5 hours, the mixture is worked up in the customary manner, giving 24.
  • 0.160 g 17 and 0.087 ml 25 are mixed in a mixture of 3.00 ml dichloroethane and 1.50 ml tetrahydrofuran with 0.026 ml acetic acid and stirred for 3 hours. After the addition of 0.188 g of 26, the mixture is stirred overnight and worked up as usual, whereby 28, the free base of 27, is obtained.
  • the hydrochloride 27 can be obtained by reaction with 1 equivalent of a 0.1 M solution of HCl in 2-propanol.
  • Ethylene glycol dimethyl ether is given 4.00 ml of an aqueous 2M sodium carbonate solution and 150.00 mg of tetrakis (triphenylphosphine) palladium (O). The mixture is refluxed for 3 hours. After cooling, the mixture is worked up as usual, giving 32.
  • acetic acid 0.10 ml of acetic acid is added to a solution of 430.00 mg of 34 and 0.210 ml of 35 in 10.0 ml of dichloroethane and 5.0 ml of tetrahydrofuran. The raction mixture is stirred for 3 hours. Then 0.50 g of sodium triacetoborohydride are added, the mixture is stirred for 2 hours and then worked up as usual, whereby the free base of 36 is obtained, from which 36 is obtained in crystalline form by addition of ethereal HCl (mp: 277 ° C. ).

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Abstract

The invention relates to the compounds of formula (I) and the salts and solvates thereof, wherein X, R1, R2, R3, R4 and R5 are defined as in claim 1. The inventive compounds are suitable as ligands of 5 HT receptors.

Description

Substituierte Pyrazole Substituted pyrazoles
Die Erfindung betrifft die Verwendung der Verbindungen der FormelThe invention relates to the use of the compounds of the formula
worin wherein
X CH oder N,X CH or N,
R1 H, A, Hai, (CH2)nHet, (CH2)nAr, Cycloalkyl mit 3 bis 7 C-Atomen,R 1 H, A, shark, (CH 2 ) n Het, (CH 2 ) n Ar, cycloalkyl with 3 to 7 C atoms,
CF3, NO2, CN, C(NH)NOH oder OCF3,CF 3 , NO 2 , CN, C (NH) NOH or OCF 3 ,
R2 (CH2)nHet, (CH2)nAr, Cycloalkyl mit 3 bis 7 C-Atomen oder CF3l R 2 (CH 2 ) n Het, (CH 2 ) n Ar, cycloalkyl with 3 to 7 C atoms or CF 3l
R3, R4 H oder einen organischen Rest, insbesondere (CH2)nCO2R5, (CH2)nCOHet, (CH2)nCON(R5)2f CHO, (CH2)πOR5, (CH2)nHet, (CH2)πN(R5)2, CH=N-OA, CH2CH=N-OA, (CH2)nNHOA, (CH2)nN(R5)Het, (CH2)nCH=N-Het, (CH2)nOCOR5, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2CH2OCF3, (CH2)nN(R5)C(R5)HCOOR5, (CH2)nN(R5)CH2COHet, (CH2)nN(R5)CH2Het, (CH2)nN(R5)CH2CH2Het, (CH2)nN(R5)CH2CH2N(R5)CH2COOR5, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2CH2N(R5)2) CH=CHCOOR5, CH=CHCH2NR5Het, CH=CHCH2N(R5)2l CH=CHCH2OR5, CH=CHCH2Het, (CH2)nN(R5)Ar, (CH2)nN(COOR5)COOR5, (CH2)nN(CONH2)COOR5, (CH2)nN(CONH2)CONH2, (CH2)nN(CH2COOR5)COOR5 I (CH2)nN(CH2CONH2)COOR5, (CH2)nN(CH2CONH2)CONH2, (CH2)nCHR5COR5, (CH2)nCHR5COOR5, (CH2)nCHR5CH2θR5, wobei jeweils einer der Reste R3 oder R4 die Bedeutung H aufweist,R 3 , R 4 H or an organic radical, in particular (CH 2 ) n CO 2 R 5 , (CH 2 ) n COHet, (CH 2 ) n CON (R 5 ) 2f CHO, (CH 2 ) π OR 5 , (CH 2 ) n Het, (CH 2 ) π N (R 5 ) 2 , CH = N-OA, CH 2 CH = N-OA, (CH 2 ) n NHOA, (CH 2 ) n N (R 5 ) Het, (CH 2 ) n CH = N-Het, (CH 2 ) n OCOR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 OCF 3 , (CH 2 ) n N (R 5 ) C (R 5 ) HCOOR 5 , (CH 2 ) nN (R 5 ) CH 2 COHet, (CH 2 ) n N (R 5 ) CH 2 Het, (CH 2 ) nN (R 5 ) CH 2 CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) CH 2 COOR 5 , ( CH 2 ) nN (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) 2) CH = CHCOOR 5 , CH = CHCH 2 NR 5 Het, CH = CHCH 2 N (R 5 ) 2l CH = CHCH 2 OR 5 , CH = CHCH 2 Het, (CH 2 ) n N (R 5 ) Ar, (CH 2 ) n N (COOR 5 ) COOR 5 , (CH 2 ) nN (CONH 2 ) COOR 5 , (CH 2 ) n N (CONH 2 ) CONH 2 , (CH 2 ) n N (CH 2 COOR 5 ) COOR 5 I (CH 2 ) nN (CH 2 CONH 2 ) COOR 5 , (CH 2 ) nN (CH 2 CONH 2 ) CONH 2 , (CH 2 ) nCHR 5 COR 5 , (CH 2 ) nCHR 5 COOR 5 , (CH 2 ) n CHR 5 CH 2 θR 5 , each one of the radicals R 3 or R 4 has the meaning H,
R5 H oder A A unsubstituiertes oder durch Hai oder CN substituiertes geradkettiges oder verzweigtes Alkyl oder Cycloalkyl mit 2 bis 4 C-Atomen, mit 1 bis 10 C-Atomen, Alkenyl mit 2 bis 10 C- Atomen, Alkoxyalkyl mit 2 bis 10 C-Atomen oder Cycloalkyl mit 4 bis 7 C-Atomen,R 5 H or A A unsubstituted or substituted by shark or CN straight-chain or branched alkyl or cycloalkyl having 2 to 4 carbon atoms, having 1 to 10 carbon atoms, alkenyl having 2 to 10 carbon atoms, alkoxyalkyl having 2 to 10 carbon atoms or cycloalkyl 4 to 7 carbon atoms,
Het einen Heteroatome enthaltenden organischen Rest, insbesondere einen unsubstituierten oder einfach oder mehrfach durch A und/oder Hai substituierten, gesättigten, ungesättigten oder aromatischen mono- oder bicyclischen heterocyclischen oder einen ein oder zwei Heteroatome enthaltenden linearen Rest mit 1 bis 15 C-Atomen,Het an organic radical containing heteroatoms, in particular an unsubstituted or mono- or polysubstituted by A and / or shark, saturated, unsaturated or aromatic mono- or bicyclic heterocyclic or a linear radical containing one or two heteroatoms and having 1 to 15 carbon atoms,
Ar einen aromatischen organischen Rest, insbesondere einen unsubstituierten oder einfach oder mehrfach durch A und/oderAr is an aromatic organic radical, in particular an unsubstituted or singly or multiply by A and / or
Hai, OR5, OOCR5, COOR5, CON(R5)2> CN, NO2, NH2) NHCOR5, CF3 oder SO2CH3 substituierten Phenylrest,Shark, OR 5 , OOCR 5 , COOR 5 , CON (R 5 ) 2> CN, NO 2 , NH 2) NHCOR 5 , CF 3 or SO 2 CH 3 substituted phenyl radical,
n 0, 1, 2, 3, 4 oder 5n 0, 1, 2, 3, 4 or 5
undand
Hai F, Cl, Br oder IShark F, Cl, Br or I
bedeuten, sowie deren Salze und Solvate, Enantiomere und Racemate, insbesondere deren physiologisch verträglichen Salze und Solvate, zur Behandlung und Prophylaxe von Krankheiten, die durch die Bindung der Verbindungen der Formel I an 5 HT-Rezeptoren beeinflusst werden können. Der Erfindung lag die Aufgabe zugrunde, Verbindungen aufzufinden, die zur Herstellung von Arzneimitteln verwendet werden können. Es wurde gefunden, daß die Verbindungen der Formel I und ihre Salze und Solvate bei guter Verträglichkeit sehr wertvolle pharmakologische Eigenschaften besitzen. Gegenstand der Erfindung sind insbesondere die in den Beispielen genannten Verbindungen, die die in der vorliegenden Anmeldung geschütertβn Eigenschaften undmean, and their salts and solvates, enantiomers and racemates, in particular their physiologically tolerable salts and solvates, for the treatment and prophylaxis of diseases which can be influenced by the binding of the compounds of the formula I to 5 HT receptors. The object of the invention was to find compounds which can be used for the production of medicaments. It has been found that the compounds of the formula I and their salts and solvates have very valuable pharmacological properties with good tolerability. The invention relates in particular to the compounds mentioned in the examples, which have the properties and properties which are described in the present application
Verwendungsmöglichkeiten der Verbindungen der Formel I aufweisen. Ähnliche Verbindungen sind beispielsweise aus DE 2201889, DE 2258033 oder DE 2906252 bekannt.Show possible uses of the compounds of formula I. Similar connections are known for example from DE 2201889, DE 2258033 or DE 2906252.
Insbesondere eignen sich die erfindungsgemäßen Verbindungen der Formel I als Liganden von 5 HT-Rezeptoren, insbesondere von 5 HT2A- und/oder 5HT2C-Rezeptoren und können in der Human- und Veterinärmedizin zur Prophylaxe und Behandlung verschiedener Krankheiten des zentralen Nervensystems, wie z.B. Schizophrenie, Depression, Demenz, Parkinsonschen Krankheit, Morbus Alzheimer, Lewy Bodies Dementia, Huntington, Tourette Syndrom, Angst, Lern- undThe compounds of the formula I according to the invention are particularly suitable as ligands of 5 HT receptors, in particular of 5 HT2A and / or 5HT2C receptors, and can be used in human and veterinary medicine for the prophylaxis and treatment of various diseases of the central nervous system, such as e.g. Schizophrenia, Depression, Dementia, Parkinson's Disease, Alzheimer's Disease, Lewy Bodies Dementia, Huntington's, Tourette's Syndrome, Anxiety, Learning and
Erinnerungseinschränkungen, neurodegenerativen Erkrankungen und anderen kognitiven Beeinträchtigungen, sowie Nikotinabhängigkeit und Schmerzen verwendet werden.Memory restrictions, neurodegenerative diseases and other cognitive impairments, as well as nicotine addiction and pain can be used.
Insbesondere bevorzugt werden die Verbindungen der Formel I und/oder ihre physiologisch unbedenklichen Salze oder Solvate zur Herstellung eines Arzneimittels zur Prophylaxe und/oder Behandlung von Psychosen, neurologischen Störungen, amyotropher Lateralskierose, Essstörungen wie Bulimie, nervöser Anorexie, des prämenstrualen Syndroms und/oder zur positiven Beeinflussung von Zwangsverhalten (obsessive-compulsive disorder, OCD) verwendet.The compounds of the formula I and / or their physiologically acceptable salts or solvates are particularly preferred for the preparation of a medicament for the prophylaxis and / or treatment of psychoses, neurological disorders, amyotrophic lateral skierosis, eating disorders such as bulimia, nervous anorexia, premenstrual syndrome and / or positive influence on obsessive-compulsive disorder (OCD).
Es wurde gefunden, dass die Verbindungen der Formel I und ihre physiologisch unbedenklichen Salze und Solvate bei guter Verträglichkeit wertvolle pharmakologische Eigenschaften besitzen, da sie Wirkungen auf dasIt has been found that the compounds of the formula I and their physiologically acceptable salts and solvates have valuable pharmacological properties with good tolerability, since they have effects on the
Zentralnervensystem besitzen. Die Verbindungen weisen eine starke Affinität zu 5-HT2A-Rezeptoren aufweisen, weiterhin zeigen sie 5-HT2A- Rezeptor-antagonistische Eigenschaften.Have a central nervous system. The compounds have a strong affinity for 5-HT 2A receptors, furthermore they show 5-HT 2A receptor antagonistic properties.
Insbesondere bevorzugt ist daher Verwendung der Verbindungen derIt is therefore particularly preferred to use the compounds of
Formel I und/oder von deren physiologisch unbedenklichen Salzen und Solvaten zur Herstellung eines Arzneimittels mit 5-HT-Rezeptor- antagonistischer Wirkung.Formula I and / or their physiologically acceptable salts and solvates for the manufacture of a medicament with 5-HT receptor antagonistic effect.
Zum in-vitro Nachweis der Affinität zu 5-HT2A-Re∑eptoren kann beispielsweise folgender Test (Beispiel A1) herangezogen werden. Die δ-HT^ Rezeptoren werden sowohl [3H]Ketanserin (eine Substanz, die für ihre Affinität zum Rezeptor bekannt ist) als auch der Testverbindung ausgesetzt. Die Abnahme der Affinität von [3H]Ketanserin zum Rezeptor ist ein Anzeichen für die Affinität der Testsubstan∑ zum 5-HT2A Rezeptor. Der Nachweis erfolgt analog der Beschreibung von J.E. Leysen et al.,The following test (example A1) can be used, for example, for in-vitro detection of the affinity for 5-HT 2A receptors. The δ-HT ^ Receptors are exposed to both [ 3 H] ketanserin (a substance known for its affinity for the receptor) and the test compound. The decrease in the affinity of [ 3 H] ketanserin for the receptor is an indication of the affinity of the test substances for the 5-HT 2 A receptor. The proof is made analogously to the description by JE Leysen et al.,
Molecular Pharmacology, 1982, 21 : 301-314 oder wie z.B. auch in EP 0320983 beschrieben.Molecular Pharmacology, 1982, 21: 301-314 or as e.g. also described in EP 0320983.
Die Wirksamkeit der erfindungsgemäßen Verbindungen als 5-HT2A Rezeptor-Antagonisten kann in vitro analog W. Feniuk et al., Mechanisms of 5-hydroxytryptamine-induced vasoconstriction, in: The Peripheral Actions of 5-Hydroxytryptamine, ed. Fozard JR, Oxford University Press, New York, 1989, p.110, gemessen werden. So wird die Kontraktilität der Rattenschwanzarterie, hervorgerufen durch 5-Hydroxytryptamin, durch 5- HT2A Rezeptoren vermittelt. Für das Testsystem werden Gefäßringe, präpariert aus der ventralen Rattenschwanzarterie, in einem Organbad mit einer sauerstoffgesättigten Lösung einer Perfusion unterzogen. Durch Eintrag ansteigender Konzentrationen an 5-Hydroxytryptamin in die Lösung erhält man eine Antwort auf die kumulative Konzentration an 5-HT. Danach wird die Testverbindung in geeigneten Konzentrationen in dasThe effectiveness of the compounds of the invention as 5-HT 2A receptor antagonists can be used in vitro analog W. Feniuk et al, Mechanisms of 5-hydroxytryptamine-induced vasoconstriction in. The Peripheral Actions of 5-Hydroxytryptamine, ed Fozard JR, Oxford. University Press, New York, 1989, p.110. The contractility of the rat tail artery, caused by 5-hydroxytryptamine, is mediated by 5-HT 2 A receptors. For the test system, vascular rings, prepared from the ventral rat tail artery, are perfused in an organ bath with an oxygen-saturated solution. A response to the cumulative concentration of 5-HT is obtained by adding increasing concentrations of 5-hydroxytryptamine to the solution. Then the test compound in suitable concentrations in the
Organbad gegeben und eine zweite Konzentrationskureve für 5-HT gemessen. Die Stärke der Testverbindung auf die Verschiebung der 5-HT induzierten Konzentrationskurve zu höheren 5-HT Konzentrationen ist ein Maß für die 5-HT2A-Rezeptor-anatgonistische Eigenschaft in vitro.Organ bath was given and a second concentration curve for 5-HT was measured. The strength of the test compound on the shift of the 5-HT induced concentration curve to higher 5-HT concentrations is a measure of the 5-HT 2A receptor anatgonistic property in vitro.
Die 5-HT2A-antagonistische Eigenschaft kann in vivo analog M.D.Serdar et al., Psychopharmacology, 1996, 128: 198-205, bestimmt werden.The 5-HT 2A antagonistic property can be determined in vivo analogously to MDSerdar et al., Psychopharmacology, 1996, 128: 198-205.
Die Verbindungen der Formel I eignen sich daher sowohl in der Veterinär- als auch in der Humanmedizin zur Behandlung von Funktionsstörungen des Zentralnervensystems sowie von Entzündungen. Sie können zur Prophylaxe und zur Bekämpfung der Folgen cerebraler Infarktgeschehen (apoplexia cerebri) wie Schlaganfall und cerebraler Ischämien sowie zur Behandlung extrapyramidal-motorischer Nebenwirkungen von Neuroleptika sowie des Morbus Parkinson, zur akuten und symptomatischen Therapie der Alzheimer Krankheit sowie zur Behandlung der amyotrophen Lateral- Sklerose verwendet werden. Ebenso eignen sie sich als Therapeutika zur Behandlung von Hirn- und Rückenmarkstraumata. Insbesondere sind sie jedoch geeignet als Arzneimittelwirkstoffe für Anxiolytika, Antidepressiva, Antipsychotika, Neuroleptika, Antihypertonika und/oder zur positiven Beeinflussung von Zwangsverhalten (obsessive-compulsive disorder,The compounds of the formula I are therefore suitable both in veterinary and in human medicine for the treatment of functional disorders of the central nervous system and of inflammation. They can be used for prophylaxis and for combating the consequences of cerebral infarction (apoplexia cerebri) such as stroke and cerebral ischemia, as well as for the treatment of extrapyramidal-motor side effects of neuroleptics and Parkinson's disease, for the acute and symptomatic therapy of Alzheimer's disease and for the treatment of amyotrophic lateral Sclerosis can be used. They are also suitable as therapeutic agents for the treatment of brain and spinal cord trauma. In particular, however, they are suitable as active pharmaceutical ingredients for anxiolytics, antidepressants, antipsychotics, neuroleptics, antihypertensives and / or for positively influencing obsessive behavior (obsessive-compulsive disorder,
OCD; z.B. WO 9524194), Angstzuständen sowie physiologischen Veränderungen, die mit Angstzuständen einhergehen wie z.B. Tachycardie, Tremor oder Schwitzen (z.B. EP 319962), Panikattacken, Psychosen, Schizophrenie, Anorexie, zwanghaften Wahnvorstellungen, Agoraphobie, Migräne, der Alzheimer Krankheit, Schlafstörungen wie auch Schlafapnoe, tardiver Dyskinesien, Lernstörungen, altersabhängiger Erinnerungsstörungen, Essstörungen wie Bulimie, Drogenmissbrauch wie z.B. von Alkohol, Opiaten, Nikotin, Psychostimulantien wie z.B. Kokain oder Amphetaminen (z.B. US 6004980), Sexualfunktionsstörungen, Schmerzuzuständen aller Art und Fibromyalgie (z.B. WO 9946245).OCD; e.g. WO 9524194), anxiety and physiological changes associated with anxiety such as Tachycardia, tremor or sweating (e.g. EP 319962), panic attacks, psychoses, schizophrenia, anorexia, compulsive delusions, agoraphobia, migraines, Alzheimer's disease, sleep disorders as well as sleep apnea, tardive dyskinesias, learning disorders, age-related memory disorders, e.g. drug abuse disorders such as bulimia disorders alcohol, opiates, nicotine, psychostimulants such as Cocaine or amphetamines (e.g. US 6004980), sexual dysfunction, all types of pain and fibromyalgia (e.g. WO 9946245).
Die Verbindungen der Formel l eignen sich zur Behandlung extrapyramidaler Nebenwirkungen (extrapyramidal side effects EPS) bei der neuroleptischen Drogentherapie. EPS ist gekennzeichnet durch Parkinson-ähnliche Syndrome, Akathisie und dystonische Reaktionen (z.B. EP 337136). Weiter sind sie geeignet zur Behandlung der nervösen Anorexie, Angina,The compounds of the formula I are suitable for the treatment of extrapyramidal side effects (EPS) in neuroleptic drug therapy. EPS is characterized by Parkinson's-like syndromes, akathisia and dystonic reactions (e.g. EP 337136). They are also suitable for the treatment of nervous anorexia, angina,
Reynaud's Phänomen, koronaren Vasospasmen, bei der Prophylaxe von Migräne (z.B. EP 208235), Schmerz und Neuralgien (z.B. EP 320983), zur Behandlung des Rett-Syndroms mit autistischen Charakterzügen, des Asperger-Syndroms, des Autismus und autistischen Störungen, bei Konzentrationsmangelzuständen, Entwicklungsstörungen, Hyperaktivitäts- zuständen mit mentaler Unterentwicklung und stereotypen Verhaltens- zuständen (z.B. WO 9524194).Reynaud's phenomenon, coronary vasospasm, in the prophylaxis of migraines (e.g. EP 208235), pain and neuralgia (e.g. EP 320983), for the treatment of Rett syndrome with autistic traits, Asperger's syndrome, autism and autistic disorders, in cases of poor concentration, Developmental disorders, hyperactivity states with mental underdevelopment and stereotypical behavioral states (eg WO 9524194).
Desweiteren sind sie geeignet zur Behandlung von endokrinen Erkran- kungen wie Hyperprolactinaemie, ferner bei Vasospasmen, thrombotischenFurthermore, they are suitable for the treatment of endocrine diseases such as hyperprolactinaemia, also for vasospasm, thrombotic
Erkrankungen (z.B. WO 9946245), Hypertension und gastrointestinalenDiseases (e.g. WO 9946245), hypertension and gastrointestinal
Erkrankungen.Diseases.
Ferner sind sie geeignet zur Behandlung cardiovaskulärer Erkrankungen sowie extrapyramidaler Symptome wie in der WO 99/11641 auf Seite 2, Zeile 24-30 beschrieben. Die erfindungsgemäßen Verbindungen eignen sich weiter zur Verminderung des Augeni,nnendruckes und zur Glaucombehandlung. Sie sind auch zur Prophylaxe und Behandlung von Vergiftungserscheinungen bei der Gabe von Ergovalin bei Tieren geeignet. Die Verbindungen eignen sich weiterhin zur Behandlung von Erkrankungen des Herz-Kreislaufsystems (WO 99/11641 , Seite 3, Zeile 14-15). Die erfindungsgemäßen Verbindungen können auch zusammen mit anderen Wirkstoffen in der Behandlung der Schizophrenie eingesetzt werden. Als andere Wirkstoffe kommen die in der WO 99/11641 auf Seite 13, Zeile 20- 26 genannten Verbindungen in Frage.They are also suitable for the treatment of cardiovascular diseases and extrapyramidal symptoms as described in WO 99/11641 on page 2, lines 24-30. The compounds according to the invention are further suitable for reducing the intraocular pressure and for glaucoma treatment. They are also suitable for the prophylaxis and treatment of poisoning symptoms when ergovalin is administered to animals. The compounds are also suitable for the treatment of diseases of the cardiovascular system (WO 99/11641, page 3, lines 14-15). The compounds according to the invention can also be used together with other active substances in the treatment of schizophrenia. Other compounds which may be used are the compounds mentioned in WO 99/11641 on page 13, lines 20-26.
Andere Verbindungen, die ebenfalls 5-HT2-antagonistische Wirkungen zeigen, sind beispielweise in der EP 0320983 beschrieben. In der WO 99/11641 sind Phenylindolderivate mit 5-HT2-antagonistischen Eigenschaften beschrieben.Other compounds which also show 5-HT 2 antagonistic effects are described, for example, in EP 0320983. WO 99/11641 describes phenylindole derivatives with 5-HT 2 -antagonistic properties.
Keines der oben genannten Dokumente beschreibt jedoch die erfindungsgemäße Verwendung der Verbindungen der Formel I als Liganden von 5 HT-Rezeptoren.However, none of the documents mentioned above describes the use according to the invention of the compounds of the formula I as ligands of 5 HT receptors.
Die Verbindungen der Formel I können als Arzneimittelwirkstoffe in der Human- und Veterinärmedizin eingesetzt werden. Ferner können sie als Zwischenprodukte zur Herstellung weiterer Arzneimittelwirkstoffe eingesetzt werden.The compounds of formula I can be used as active pharmaceutical ingredients in human and veterinary medicine. They can also be used as intermediates for the production of further active pharmaceutical ingredients.
Gegenstand der Erfindung ist dementsprechend die Verwendung der Verbindungen der Formel I in der Human- und Tiermedizin.The invention accordingly relates to the use of the compounds of the formula I in human and veterinary medicine.
Ein weiterer Gegenstand sind die neuen Verbindungen der Formel I.Another subject is the new compounds of formula I.
Die Verbindungen der Formel l werden vorzugsweise dadurch hergestellt, daß man zunächst eine Verbindung der Formel IIThe compounds of formula I are preferably prepared by firstly preparing a compound of formula II
oder deren Säureadditionssalze worin or their acid addition salts in which
R1 und X die oben angegebenen Bedeutungen haben, mit einer Verbindung der Formel IIIR 1 and X have the meanings given above, with a compound of the formula III
worin wherein
A und R2 die oben angegebenen Bedeutungen haben, zu einer Verbindung der Formel IAA and R 2 have the meanings given above, to a compound of the formula IA
umsetzt implements
oder dadurch, daß man eine Verbindung der Formel IIor in that a compound of formula II
oder deren Säureadditionssalze worinor their acid addition salts in which
R1 und X die oben angegebenen Bedeutungen haben, mit einer Verbindung der Formel IVR 1 and X have the meanings given above, with a compound of the formula IV
worin A und R2 die oben angegebenen Bedeutungen haben, zu einer Verbindung der Formel IB wherein A and R 2 have the meanings given above, to a compound of the formula IB
umsetzt und die Verbindungen der Formeln IA und IB dann durch übliche Methoden in die weiteren Verbindungen der Formel I überführt. and the compounds of the formulas IA and IB are then converted into the further compounds of the formula I by customary methods.
Insbesondere können die Verbindungen der Formel IA und IB durch Anwendung von Reduktionsmitteln wie z.B. Lithiumaluminiumhydrid in die entsprechenden Alkohole der Formeln IC und IDIn particular, the compounds of formula IA and IB can be obtained by using reducing agents such as e.g. Lithium aluminum hydride in the corresponding alcohols of the formulas IC and ID
überführt werden, die z.B. mit MnO zu den Verbindungen IE und IF oxidiert werden können. are transferred, which can be oxidized, for example, with MnO to the compounds IE and IF.
Die Verbindungen der Formeln IE und IF können ihrerseits nach bekannten Verfahren mit entsprechenden Nucleophilen wie z.B. Stickstoffbasen, insbesondere Hydroxylamin, O-Methylhydroxylamin, Morpholin, Piperidin, Pipera∑in, N-ivlethylpiperazin, 4-Methylpipera∑in-1-ylarnin, Pyrrolidin, Pyrazolidin oder Imida∑olidin, gegebenenfalls in Gegenwart eines Reduktionsmittels wie Natriumtriacetoxyborhydrid aminiert oder zu den entsprechenden Iminen umgesetzt werden. Weiterhin können die Verbindungen der Formeln IE und IF durch Wittig-Reaktion mit Methoxymethyltriphenylphosphoniumsalzen zu den entsprechenden Enolethern umgesetzt werden, die durch Behandlung mit einer Säure in die homologisierten Aldehyde IG und IH The compounds of the formulas IE and IF can in turn be prepared using known nucleophiles, such as nitrogen bases, in particular hydroxylamine, O-methylhydroxylamine, morpholine, piperidine, piperain, N-ivlethylpiperazine, 4-methylpiperain-1-ylarnine, pyrrolidine, Pyrazolidine or Imida∑olidin, optionally aminated in the presence of a reducing agent such as sodium triacetoxyborohydride or reacted to the corresponding imines. Furthermore, the compounds of the formulas IE and IF can be converted by Wittig reaction with methoxymethyltriphenylphosphonium salts to the corresponding enol ethers, which by treatment with an acid in the homologated aldehydes IG and IH
überführt werden können. Die Verbindungen der Formel IG und IH können analog zu den Verbindungen der Fomeln IE und IF zu den weiteren Verbindungen der Formel I umgesetzt werden. can be transferred. The compounds of the formulas IG and IH can be converted analogously to the compounds of the formulas IE and IF to the further compounds of the formula I.
Unter Solvaten der Verbindungen der Formel I werden Anlagerungen von inerten Lösungsmittelmolekülen an die Verbindungen der Formel I verstanden, die sich aufgrund ihrer gegenseitigen Anziehungskraft ausbilden. Solvate sind z.B. Mono- oder Dihydrate oder Alkoholate.Solvates of the compounds of the formula I are understood to mean the addition of inert solvent molecules to the compounds of the formula I, which are formed on account of their mutual attraction. Solvates are e.g. Mono- or dihydrates or alcoholates.
Vor- und nachstehend haben die Reste X, A, Ar, Het, n, R1, R2, R3, R4 und R5 die bei der Formel I angegebenen Bedeutungen, sofern nicht ausdrücklich etwas anderes angegeben ist.Above and below, the radicals X, A, Ar, Het, n, R 1 , R 2 , R 3 , R 4 and R 5 have the meanings given in the formula I, unless expressly stated otherwise.
X bedeutet vorzugsweise CH. R1 steht bevorzugt für A, Hai, (CH2)nHet oder (CH2)nAr, insbesondere für A, (CH2)nHet oder (CH2)nAr. Ganz besonders bevorzugt bedeutet R1 Phenyl, 2-, 3- oder 4-Cyanophenyl, 2-, 3- oder 4-Fluorphenyl, 2-, 3- oder 4-Methyl-, Ethyl-, n-Propyl- oder n-Butylphenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5- oder 3,6-Difluor- , Dichlor- oder Dicyanophenyl, 3,4,5-Trifluorphenyl, 3,4,5-X is preferably CH. R 1 preferably represents A, shark, (CH 2 ) n Het or (CH 2 ) n Ar, in particular A, (CH 2 ) n Het or (CH 2 ) n Ar. R 1 very particularly preferably denotes phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl-, ethyl-, n-propyl- or n-butylphenyl , 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5- or 3,6-difluoro-, dichloro- or dicyanophenyl, 3,4,5-trifluorophenyl , 3,4,5-
Trimethoxy- oder Triethoxyphenyl, Thiophen-2-yl oder Thiophen-3-yl oder 1-, 2- oder 3-Pyrrolyl.Trimethoxy- or triethoxyphenyl, thiophene-2-yl or thiophene-3-yl or 1-, 2- or 3-pyrrolyl.
R2 bedeutet vorzugsweise (CH2)nHet, (CH2)nNHA, (CH2)nNHCH2Het oder (CH2)nAr, insbesondere (CH2)nHet, (CH2)nNHA, (CH2)nNHCH2Het. Ganz besonders bevorzugt bedeutet R2 Phenyl, 2-, 3- oder 4-Cyanophenyl, 2-, 3- oder 4-Fluorphenyl, 2-, 3- oder 4-Methyl-, Ethyl-, n-Propyl- oder n- Butylphenyl, 2,3-, 2,4-, 2,5-, 2,6-Difluor- oder Dicyanophenyl, Thiophen-2-yl oder Thiophen-3-yl, 2-, 3- oder 4-Pyridyl, 2-, 4- oder 5-Oxazolyl, 2-, 4- oder 5-Thiazolyl, Chinolinyl, Isochinolinyl, 2- oder 4-Pyridazyl, 2-, 4- oder 5-R 2 preferably denotes (CH 2 ) n Het, (CH 2 ) nNHA, (CH 2 ) nNHCH 2 Het or (CH 2 ) n Ar, in particular (CH 2 ) n Het, (CH 2 ) n NHA, (CH 2 ) n NHCH 2 Het. R 2 very particularly preferably denotes phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl-, ethyl-, n-propyl- or n-butylphenyl , 2,3-, 2,4-, 2,5-, 2,6-difluoro- or dicyanophenyl, thiophene-2-yl or thiophene-3-yl, 2-, 3- or 4-pyridyl, 2-, 4- or 5-oxazolyl, 2-, 4- or 5-thiazolyl, quinolinyl, isoquinolinyl, 2- or 4-pyridazyl, 2-, 4- or 5-
Pyrimidyl, 2- oder 3-Pyrazinyl, 2- oder 3-Furyl.Pyrimidyl, 2- or 3-pyrazinyl, 2- or 3-furyl.
Sofern R3 H bedeutet, weist R4 bevorzugt die Bedeutung (CH2)nCO2R5, (CH2)n-Het, (CH2)πNHA, (CH2)nNHCH2-Het, (CH2)nCO-Het, CHO, CH2OR5, (CH2)nN(R5)2 oder CH=N-OA, insbesondere aber (CH2)nCO2R5, (CH2)nCO-If R 3 is H, R 4 preferably has the meaning (CH 2 ) nCO 2 R 5 , (CH 2 ) n -Het, (CH 2 ) π NHA, (CH 2 ) n NHCH 2 -Het, (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n N (R 5 ) 2 or CH = N-OA, but especially (CH 2 ) nCO 2 R 5 , (CH 2 ) n CO-
Het, CHO, CH=N-OA oder (CH2)n-Het auf. Sofern R4 H bedeutet, weist R3 bevorzugt die Bedeutung (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het, (CH2)πN(R5)2 oder CH=N-OA, (CH2)nN(R5)Het, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2Het, (CH2)nN(R5)CH2CH2Het, (CH2)nN(R5)CH2CH2N(R5)2, CH=CHCH2NR5Het, CH=CHCH2N(R5)2,Het, CHO, CH = N-OA or (CH 2 ) n -Het. If R 4 is H, R 3 preferably has the meaning (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) πN (R 5 ) 2 or CH = N-OA, (CH 2 ) n N (R 5 ) Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) 2 , CH = CHCH 2 NR 5 Het , CH = CHCH 2 N (R 5 ) 2 ,
CH=CHCH2OR5, CH=CHCH2Het oder (CH2)nN(R5)Ar, insbesondere aber (CH2)nHet, (CH2)nN(R5)2, (CH2)nN(R5)Het, (CH2)πN(R5)CH2CH2OR5, (CH2)nN(R5)CH2Het, (CH2)nN(R5)CH2CH2Het, (CH2)πN(R5)CH2CH2N(R5)2, CH=CHCH2NR5Het, CH=CHCH2N(R5)2, CH=CHCH2OR5, CH=CHCH2Het, (CH2)nN(R5)Ar auf. Weitere bevorzugte Bedeutungen der Reste R3 ergeben sich aus den Bespielen. Besonders bevorzugt bedeutet R4 H.CH = CHCH 2 OR 5 , CH = CHCH 2 Het or (CH 2 ) n N (R 5 ) Ar, but especially (CH 2 ) n Het, (CH 2 ) n N (R 5 ) 2 , (CH 2 ) n N (R 5 ) Het, (CH 2 ) π N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 Het, (CH 2 ) π N (R 5 ) CH 2 CH 2 N (R 5 ) 2 , CH = CHCH 2 NR 5 Het, CH = CHCH 2 N (R 5 ) 2 , CH = CHCH 2 OR 5 , CH = CHCH 2 Het, (CH 2 ) n N (R 5 ) Ar. Further preferred meanings of the R 3 radicals result from the examples. R 4 particularly preferably denotes H.
R5 weist vorzugsweise die Bedeutung A auf.R 5 preferably has the meaning A.
A bedeutet bevorzugt Alkyl, ist vorzugsweise unverzweigt und hat 1 , 2, 3,A is preferably alkyl, is preferably unbranched and has 1, 2, 3,
4, 5, 6, 7, 8, 9 oder 10 C-Atome, vorzugsweise 1 , 2, 3, 4, 5 oder 6 C-Atome und bedeutet vorzugsweise Methyl, Ethyl, n-oder Propyl, weiterhin bevorzugt lsopropyl, Butyl, Isobutyl, sek.-Butyl oder tert.-Butyl, aber auch n-Pentyl, neo-Pentyl, Isopentyl oder n-Hexyl. Besonders bevorzugt ist Methyl, Ethyl, n-Propyl, Isopro'pyl, n-Butyl, n-Pentyl, n-Hexyl oder n-Decyl.4, 5, 6, 7, 8, 9 or 10 carbon atoms, preferably 1, 2, 3, 4, 5 or 6 carbon atoms and preferably means methyl, ethyl, n- or propyl, further preferably isopropyl, butyl, isobutyl, sec-butyl or tert-butyl, but also n-pentyl, neopentyl, isopentyl or n-hexyl. Is particularly preferably methyl, ethyl, n-propyl, isopropyl 'pyl, n-butyl, n-pentyl, n-hexyl or n-decyl.
Femer weist A bevorzugt die Bedeutung der Gruppe (CH2)mOCH3 oder (CH2)mC2H5 auf, worin m 2, 3, 4, 5 oder 6, insbesondere aber 2 bedeutet.A also preferably has the meaning of the group (CH 2 ) m OCH 3 or (CH 2 ) m C 2 H 5 , where m is 2, 3, 4, 5 or 6, but in particular 2.
Sofern A Alkenyl bedeutet, steht es vorzugsweise für Allyl, 2- oder 3- Butenyl, Isobutenyl, sek.-Butenyl, ferner bevorzugt ist 4-Pentenyl, iso-If A is alkenyl, it is preferably allyl, 2- or 3-butenyl, isobutenyl, sec-butenyl, 4-pentenyl, iso-
Pentenyl oder 5-Hexenyl.Pentenyl or 5-hexenyl.
Het ist vorzugsweise ein unsubstituierter oder durch A substituierter aromatischer und insbesondere gesättigter heterocyclischer Rest. Bevorzugt bedeutet Het 1-Piperidyl, 1-Piperazyl, 1-(4-Methyl)-piperazyl, 4-Het is preferably an unsubstituted or aromatic and in particular saturated heterocyclic radical which is substituted by A. Het preferably denotes 1-piperidyl, 1-piperazyl, 1- (4-methyl) -piperazyl, 4-
Methylpiperazin-1-ylamin, 4-Morpholinyl, 1-Pyrrolidinyl, 1-Pyrazolidinyl 1-(2-Methyl)-pyrazolidinyl, 1-lmidazoiidinyl oder 1-(3-Methyl)- imidazolidinyl,Thiophen-2-yl oder Thiophen-3-yl, 2-, 3- oder 4-Pyridyl, das unsubstituiert oder durch eine oder mehrere CN-Gruppe substituiert sein kann, 2-, 4- oder 5-Oxazolyl, 2-, 4- oder 5-Thiazolyl, Chinolinyl,Methylpiperazin-1-ylamine, 4-morpholinyl, 1-pyrrolidinyl, 1-pyrazolidinyl 1- (2-methyl) -pyrazolidinyl, 1-imidazoiidinyl or 1- (3-methyl) imidazolidinyl, thiophene-2-yl or thiophene-3 -yl, 2-, 3- or 4-pyridyl, which may be unsubstituted or substituted by one or more CN groups, 2-, 4- or 5-oxazolyl, 2-, 4- or 5-thiazolyl, quinolinyl,
Isochinolinyl, 2- oder 4-Pyridazyl, 2-, 4- oder 5-Pyrimidyl, 2- oder 3- Pyrazinyl. Weiterhin bedeutet Het bevorzugt einen Rest aus der folgenden Tabelle:Isoquinolinyl, 2- or 4-pyridazyl, 2-, 4- or 5-pyrimidyl, 2- or 3-pyrazinyl. Het also preferably means a radical from the following table:
Besonders bevorzugt bedeutet Het einen der folgenden Reste:Het is particularly preferably one of the following radicals:
Ar bedeutet vorzugsweise einen unsubstituierten oder durch Hai, OH, CN,Ar preferably denotes an unsubstituted or by shark, OH, CN,
NO3 NH2, NHCOCH3, COOCH3 CONH2 oder CF3 substituierten Phenylrest. Vorzugsweise ist Ar in 4- oder 3-Position substituiert.NO 3 NH 2 , NHCOCH 3 , COOCH 3 CONH 2 or CF 3 substituted phenyl radical. Ar is preferably substituted in the 4- or 3-position.
n bedeutet vorzugsweise 0, 1 oder 2, insbesondere 0 oder 1. Cycloalkyl hat vorzugsweise 3-7 C-Atome und steht bevorzugt für Cyclo- propyl und Cyclobutyl, weiterhin bevorzugt für Cyclopentyl oder Cyclo- hexyl, ferner auch für Cycloheptyl, besonders bevorzugt ist Cyclopentyl.n is preferably 0, 1 or 2, in particular 0 or 1. Cycloalkyl preferably has 3-7 C atoms and preferably represents cyclopropyl and cyclobutyl, further preferably cyclopentyl or cyclohexyl, furthermore also cycloheptyl, cyclopentyl is particularly preferred.
Hai bedeutet vorzugsweise F, Cl oder Br, aber auch I.Shark preferably means F, Cl or Br, but also I.
Sofern die Verbindungen der Formel I ein oder mehrere chirale C-Atome aufweist, sind die Enantiomeren, Diastereomere und deren Mischungen Gegenstand der vorliegenden Erfindung.If the compounds of the formula I have one or more chiral carbon atoms, the enantiomers, diastereomers and mixtures thereof are the subject of the present invention.
Für die gesamte Erfindung gilt, daß sämtliche Reste, die mehrfach auftreten, gleich oder verschieden sein können, d.h. unabhängig voneinander sind.It applies to the entire invention that all residues which occur more than once can be the same or different, i.e. are independent of each other.
Dementsprechend sind Gegenstand der Erfindung insbesondere diejenigen Verbindungen der Formel I, in denen mindestens einer der genannten Reste eine der vorstehend angegebenen bevorzugten Bedeutungen hat. Einige bevorzugte Gruppen von Verbindungen können durch die folgenden Teilformeln 11 bis 19 ausgedrückt werden, die der Formel I entsprechen und worin die nicht näher bezeichneten Reste die bei der Formel I angegebeneAccordingly, the invention relates in particular to those compounds of the formula I in which at least one of the radicals mentioned has one of the preferred meanings indicated above. Some preferred groups of compounds can be expressed by the following partial formulas 11 to 19, which correspond to the formula I and in which the radicals which are not specified are those given in the formula I.
Bedeutung haben, worin jedochHave meaning, however
in 11 R1 (CH2)nHet oder (CH2)πAr bedeuten;in 11 R 1 is (CH 2 ) n Het or (CH 2 ) π Ar;
in !2 R1 (CH2)πHet oder (CH2)nArin! 2 R 1 (CH 2 ) π Het or (CH 2 ) n Ar
R2 (CH2)nAr bedeuten;R 2 is (CH 2 ) n Ar;
in l3 R1 (CH2)nAr R2 (CH2)nAr bedeuten;in 13 R 1 is (CH 2 ) n Ar R 2 (CH 2 ) n Ar;
in 14 R1 (CH2)nHet oder (CH2)nArin 14 R 1 (CH 2 ) n Het or (CH 2 ) n Ar
R2 (CH2)πAr R4 H R3 (CHzJn-Het, (CH2)nNHA, (CH2)nNHCH2-Het, (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het, (CH2)nN(R5)2 oder CH=N-OA bedeuten;R 2 (CH 2 ) π Ar R 4 H R 3 (CHzJn-Het, (CH 2 ) n NHA, (CH 2 ) n NHCH 2 -Het, (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) n N (R 5 ) 2 or CH = N-OA;
in 15 R1 (CH2)nHet oder (CH2)nAr R2 (CH2)nAr R4 Hin 15 R 1 (CH 2 ) n Het or (CH 2 ) n Ar R 2 (CH 2 ) n Ar R 4 H
R3 (CH2)n-Het, (CH2)nNHA, (CH2)πNHCH2-Het, (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het, (CH2)nN(R5)2 oder CH=N-OA R5 H, Methyl, Ethyl, n-Propyl, Isopropyl, n-Butyl, n-Pentyl, n-R 3 (CH 2 ) n -Het, (CH 2 ) n NHA, (CH 2 ) π NHCH 2 -Het, (CH 2 ) nCO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) n N (R 5 ) 2 or CH = N-OA R 5 H, methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n -
Hexyl oder n-Decyl bedeuten;Mean hexyl or n-decyl;
in 16 R1 (CH2)nHet oder (CH2)nAr R2 (CH2)πAr R4 Hin 16 R 1 (CH 2 ) n Het or (CH 2 ) n Ar R 2 (CH 2 ) π Ar R 4 H
R3 (CH2)n-Het, (CH2)nNHA, (CH2)πNHCH2-Het, (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het, (CH2)nN(R5)2 oder CH=N-OA R5 H, Methyl, Ethyl, n-Propyl, Isopropyl, n-Butyl, n-Pentyl, n-R 3 (CH 2 ) n -Het, (CH 2 ) n NHA, (CH 2 ) π NHCH 2 -Het, (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) n N (R 5 ) 2 or CH = N-OA R 5 H, methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n-
Hexyl oder n-Decyl n 0, 1 oder 2 bedeuten;Hexyl or n-decyl n is 0, 1 or 2;
in 17 R1 (CH2)nHet oder (CH2)nAr R2 (CH2)nAr R3 H R4 (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het,in 17 R 1 (CH 2 ) n Het or (CH 2 ) n Ar R 2 (CH 2 ) n Ar R 3 HR 4 (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het,
(CH2)nN(R5)2 oder CH=N-OA bedeuten;(CH 2 ) n is N (R 5 ) 2 or CH = N-OA;
in 18 R1 (CH2)nHet oder (CH2)nAr R2 (CH2)nArin 18 R 1 (CH 2 ) n Het or (CH 2 ) n Ar R 2 (CH 2 ) n Ar
R3 H R4 (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)π-Het,R 3 H R 4 (CH 2 ) nCO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) π -Het,
(CH2)nN(R5)2 oder CH=N-OA R5 H, Methyl, Ethyl, n-Propyl, Isopropyl, n-Butyl, n-Pentyl, n-(CH 2 ) n N (R 5 ) 2 or CH = N-OA R 5 H, methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n-
Hexyl oder n-Decyl bedeuten;Mean hexyl or n-decyl;
in 19 R1 (CH2)nHet oder (CH2)nAr R2 (CH2)nAr R3 H R4 (CH2)nC02R5, (CH2)XO-Het, CHO, CH2OR5, (CH2)n-Hetin 19 R 1 (CH 2 ) n Het or (CH 2 ) n Ar R 2 (CH 2 ) n Ar R 3 HR 4 (CH 2 ) n C0 2 R 5 , (CH 2 ) XO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het
(CH2)πN(R5)2 oder CH=N-OA R5 H, Methyl, Ethyl, n-Propyl, Isopropyl, n-Butyl, n-Pentyl, n-(CH 2 ) πN (R 5 ) 2 or CH = N-OA R 5 H, methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n-
Hexyl oder n-Decyl n 0, 1 oder 2 bedeuten;Hexyl or n-decyl n is 0, 1 or 2;
Ganz besonders bevorzugt sind die Verbindungen der Formeln a bis o:The compounds of the formulas a to o are very particularly preferred:
[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-ylmethyl]- (a)[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] - (a)
(4-methyl-piperazin-1-yl)-amin(4-methyl-piperazin-1-yl) -amine
4-{2-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl]- (b) ethyl -morpholin4- {2- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl] - (b) ethyl-morpholine
4-{3-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl]- (c) allylj-morpholin4- {3- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl] - (c) allylj-morpholine
1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (d) ylmethyl]-pyrrolidin-3-ol1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (d) ylmethyl] pyrrolidin-3-ol
1 -[1 -(4'-Fluoro-biphenyi-4~yl)-5-(2-fluoro-phenyl)-1 H- (e) pyrazol-4-ylmethyl]-4-methyl-piperazin 1-[5-(2-Fluoro-phenyl)-1-(4-thiophen-3-yl-phenyl)-1 H- (f) pyrazol-4-ylmethyl]-4-methyl-piperazin1 - [1 - (4'-Fluoro-biphenyi-4 ~ yl) -5- (2-fluoro-phenyl) -1 H- (e) pyrazol-4-ylmethyl] -4-methyl-piperazine 1- [5 - (2-Fluoro-phenyl) -1- (4-thiophene-3-yl-phenyl) -1 H- (f) pyrazol-4-ylmethyl] -4-methyl-piperazine
1 -[5-Furan-2-yl-1 -(4-thiophen-3-yl-phenyl)-1 H-pyrazol-4- (g) ylmethyl]-4-methyl-piperazin N1-[1-Biphenyl-4-yl-5-(2-fluoro-phβnyl)-1H-pyrazol-4- (h) ylmethyl]-ethan-1 ,2-diamin 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (i) ylmethyl]-amino}-ethanol1 - [5-Furan-2-yl-1 - (4-thiophene-3-yl-phenyl) -1 H -pyrazol-4- (g) ylmethyl] -4-methylpiperazine N 1 - [1-biphenyl -4-yl-5- (2-fluoro-phβnyl) -1H-pyrazol-4- (h) ylmethyl] -ethane-1,2-diamine 2 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (i) ylmethyl] amino} ethanol
[1 -Biphenyl-4-yl-5-(2-f luoro-phenyl)-1 H-pyra∑ol-4-ylmethy I]- (j)[1 -Biphenyl-4-yl-5- (2-f luoro-phenyl) -1 H-pyra∑ol-4-ylmethy I] - (j)
(2-methoxy-βthyl)-amin 2-{[1-Biphβnyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- (k) ylmethyO-methyl-aminoJ-ethanol(2-methoxy-βthyl) amine 2 - {[1-Biphβnyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- (k) ylmethyO-methylaminoJ-ethanol
1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (I) ylmethyl]-4-methyl-[1 ,4]diazepam 1-[1-(4'-Fluoro-biphenyl-4-yl)-5-phenyl-1H-pyrazol-4- (m) ylmethyl]-4-methyl-piperazin1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (I) ylmethyl] -4-methyl- [1, 4] diazepam 1- [1- ( 4'-fluoro-biphenyl-4-yl) -5-phenyl-1H-pyrazol-4- (m) ylmethyl] -4-methyl-piperazine
1-[5-(2-Fluoro-phenyl)-1-(4-pyrrol-1-yl-phenyI)-1H-pyrazol- (n)1- [5- (2-Fluoro-phenyl) -1- (4-pyrrol-1-yl-phenyI) -1H-pyrazole- (n)
4-ylmethyl]-4-methyl-piperazin4-ylmethyl] -4-methyl-piperazine
[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4-ylmethyl]- (o) methyl-(1-methyl-pyrrolidin-3-yl)-amin[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4-ylmethyl] - (o) methyl- (1-methyl-pyrrolidin-3-yl) amine
Die Verbindungen der Formel I und auch die Ausgangsstoffe zu ihrer Herstellung werden im übrigen nach an sich bekannten Methoden hergestellt, wie sie in der Literatur (z.B. in den Standardwerken wie Houben- Weyl, Methoden der organischen Chemie, Georg-Thieme-Verlag, Stuttgart), beschrieben sind, und zwar unter Reaktionsbedingungen, die für die genannten Umsetzungen bekannt und geeignet sind. Dabei kann man auch von an sich bekannten, hier nicht näher erwähnten Varianten Gebrauch machen. Die Verbindung der Formel III wird vorzugsweise durch Umsetzung vonThe compounds of the formula I and also the starting materials for their preparation are otherwise prepared by methods known per se, as described in the literature (for example in the standard works such as Houben-Weyl, methods of organic chemistry, Georg-Thieme-Verlag, Stuttgart) , are described, namely under reaction conditions which are known and suitable for the reactions mentioned. Use can also be made of variants which are known per se and are not mentioned here in detail. The compound of formula III is preferably by reacting
Verbindungen der Formel VCompounds of formula V
worin A die oben angegebene Bedeutung aufweist, mit Verbindungen der Formel VI wherein A has the meaning given above, with compounds of the formula VI
worin R2 und A die oben angegebene Bedeutung aufweisen, unter für derartige Reaktionen bekannten Bedingungen erhalten. wherein R 2 and A have the meaning given above, obtained under conditions known for such reactions.
Die Ausgangsstoffe können, falls erwünscht, auch in situ gebildet werden, so daß man sie aus dem Reaktionsgemisch nicht isoliert, sondern sofort weiter zu den Verbindungen der Formel I umsetzt.If desired, the starting materials can also be formed in situ, so that they are not isolated from the reaction mixture, but instead are immediately reacted further to give the compounds of the formula I.
Andererseits ist es möglich, die Reaktion stufenweise durchzuführen.On the other hand, it is possible to carry out the reaction in stages.
Die Ausgangsstoffe der Formeln II, III und IV sind in der Regel bekannt. Sofern sie nicht bekannt sind, können sie nach an sich bekannten Methoden hergestellt werden.The starting materials of formulas II, III and IV are generally known. If they are not known, they can be produced by methods known per se.
Im einzelnen erfolgen die Umsetzungen der Verbindungen der Formel II mit den Verbindungen der Formel III und den Verbindungen der Formel IV in Gegenwart oder Abwesenheit eines vorzugsweise inerten Lösungsmittels bei Temperaturen zwischen etwa -20 und etwa 150°, vorzugsweise zwischen 20 und 100°.In particular, the reactions of the compounds of the formula II with the compounds of the formula III and the compounds of the formula IV are carried out in the presence or absence of a preferably inert solvent at temperatures between about -20 and about 150 °, preferably between 20 and 100 °.
Als inerte Lösungsmittel eignen sich z.B. Kohlenwasserstoffe wie Hexan, Petrolether, Benzol, Toluol oder Xylol; chlorierte Kohlenwassertoffe wie Trichlorethylen, 1 ,2-Dichlorethan .Tetrachlorkohlenstoff, Chloroform oderSuitable inert solvents are e.g. Hydrocarbons such as hexane, petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons such as trichlorethylene, 1, 2-dichloroethane, carbon tetrachloride, chloroform or
Dichlormethan; Alkohole wie Methanol, Ethanol, Isopropanol, n-Propanol, n-Butanol oder tert.-Butanol; Ether wie Diethylether, Diisopropylether, Tetrahydrofuran (THF) oder Dioxan; Glykolether wie Ethylenglykolmono- methyl- oder -monoethylether (Methylglykol oder Ethylglykol), Ethylen- glykoldimethylether (Diglyme); Ketone wie Aceton oder Butanon; Amide wie Acetamid, Dimethylacetamid oder Dimethylformamid (DMF); Nitrile wie Acetonitril; Sulfoxide wie Dimethylsulfoxid (DMSO); Nitroverbindungen wie Nitromethan oder Nitrobenzol; Ester wie Ethylacetat oder Gemische der genannten Lösungsmittel.dichloromethane; Alcohols such as methanol, ethanol, isopropanol, n-propanol, n-butanol or tert-butanol; Ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran (THF) or dioxane; Glycol ethers such as ethylene glycol monomethyl or monoethyl ether (methyl glycol or ethyl glycol), ethylene glycol dimethyl ether (diglyme); Ketones such as acetone or butanone; Amides such as acetamide, dimethylacetamide or dimethylformamide (DMF); Nitriles such as acetonitrile; Sulfoxides such as dimethyl sulfoxide (DMSO); Nitro compounds such as nitromethane or nitrobenzene; Esters such as ethyl acetate or mixtures of the solvents mentioned.
Der für die Umsetzung erforderliche pH-Wert kann in Anlehnung an für ähnliche Umsetzungen von Carbonyl- mit Aminoverbindungen gewählte pH-Werte eingestellt werden. Vorzugsweise wird der pH-Wert durch die Verwendung des jeweiligen Säureadditionssalzes vorzugsweise eines Halogenwasserstoff-Additionssalzes der Verbindung der Formel II vorgegeben, d.h. es erfolgt keine zusätzliche Basen- oder Säurezugabe zur Reaktionsmichung. Bevorzugte Säureadditionssalze sind Hydrochloride oder -bromideThe pH value required for the reaction can be adjusted on the basis of pH values selected for similar reactions of carbonyl with amino compounds. The pH is preferably predetermined by the use of the respective acid addition salt, preferably a hydrogen halide addition salt of the compound of the formula II, ie there is no additional base or acid addition for reaction mix. Preferred acid addition salts are hydrochlorides or bromides
Eine Base der Formel I kann mit einer Säure in das zugehörige Säure- additionssalz übergeführt werden, beispielsweise durch Umsetzung äquivalenter Mengen der Base und der Säure in einem inerten Lösungsmittel wie Ethano! und anschließendes Eindampfen. Für diese Umsetzung kommen insbesondere Säuren in Frage, die physiologisch unbedenkliche Salze liefern. So können anorganische Säuren verwendet werden, z.B. Schwefelsäure, Salpetersäure, Halogenwasserstoffsäuren wie Chlorwasserstoffsäure oder Bromwasserstoffsäure, Phosphorsäuren wie Ortho- phosphorsäure, Sulfaminsäure, ferner organische Säuren, insbesondere aliphatische, alicyclische, araliphatische, aromatische oder heterocyclische ein- oder mehrbasige Carbon-, Sulfon- oder Schwefelsäuren, z.B. Ameisensäure, Essigsäure, Propionsäure, Pivalinsäure, Diethylessigsäure,A base of the formula I can be converted into the associated acid addition salt using an acid, for example by reacting equivalent amounts of the base and the acid in an inert solvent such as ethano! and then evaporating. In particular, acids that provide physiologically acceptable salts are suitable for this implementation. So inorganic acids can be used, e.g. Sulfuric acid, nitric acid, hydrohalic acids such as hydrochloric acid or hydrobromic acid, phosphoric acids such as orthophosphoric acid, sulfamic acid, also organic acids, especially aliphatic, alicyclic, araliphatic, aromatic or heterocyclic mono- or polybasic carboxylic, sulfonic or sulfuric acids, e.g. Formic acid, acetic acid, propionic acid, pivalic acid, diethyl acetic acid,
Malonsäure, Bernsteinsäure, Pimelinsäure, Fumarsäure, Maleinsäure, Milchsäure, Weinsäure, Äpfelsäure, Citronensäure, Gluconsäure, Ascor- binsäure, Nicotinsäure, Isonicotinsäure, Methan- oder Ethansulfonsäure, Ethandisulfonsäure, 2-Hydroxyethansulfonsäure, Benzolsulfonsäure, p- Toluolsulfonsäure, Naphthalin-mono- und -disulfonsäuren, Lauryl- schwefelsäure. Salze mit physiologisch nicht unbedenklichen Säuren, z.B. Pikrate, können zur Isolierung und /oder Aufreinigung der Verbindungen der Formel I verwendet werden.Malonic acid, succinic acid, pimelic acid, fumaric acid, maleic acid, lactic acid, tartaric acid, malic acid, citric acid, gluconic acid, ascorbic acid, nicotinic acid, isonicotinic acid, methane- or ethanesulfonic acid, ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic, naphthalene-mono- and -disulfonic acids, lauryl-sulfuric acid. Salts with physiologically unacceptable acids, e.g. Picrates can be used for the isolation and / or purification of the compounds of the formula I.
Andererseits können, falls gewünscht, die freien Basen der Formel I aus ihren Salzen mit Basen (z.B. Natrium- oder Kaliumhydroxid oder -carbonat) in Freiheit gesetzt werden.On the other hand, if desired, the free bases of formula I can be liberated from their salts with bases (e.g. sodium or potassium hydroxide or carbonate).
Bevorzugter Gegenstand der Erfindung ist die Verwendung der Verbindungen der Formel I und/oder ihrer physiologisch unbedenklichenThe preferred object of the invention is the use of the compounds of formula I and / or their physiologically acceptable
Salze und/oder Solvate zur Herstellung pharmazeutischer Zubereitungen, zur Behandlung oder Prophylaxe von Krankheiten, die durch die Bindung der Verbindungen der Formel I an 5 HT-Rezeptoren beeinflußt werden können, insbesondere auf nicht-chemischem Wege. Hierbei können sie zusammen mit mindestens einem festen, flüssigen und/oder halbflüssigenSalts and / or solvates for the production of pharmaceutical preparations, for the treatment or prophylaxis of diseases which can be influenced by the binding of the compounds of the formula I to 5 HT receptors, in particular in a non-chemical way. They can be used together with at least one solid, liquid and / or semi-liquid
Träger- oder Hilfsstoff und gegebenenfalls in Kombination mit einem oder mehreren weiteren Wirkstoffen in eine geeignete Dosierungsform gebracht werden.Carrier or auxiliary and optionally in combination with an or several other active ingredients are brought into a suitable dosage form.
Gegenstand der Erfindung sind ferner pharmazeutische Zubereitungen, enthaltend mindestens eine Verbindung der Formel I und/oder eines ihrer physiologisch unbedenklichen Salze und/oder Solvate zur Behandlung oder Prophylaxe von Krankheiten, die durch die Bindung der Verbindungen der Formel I an 5 HT-Rezeptoren beeinflußt werden.The invention further relates to pharmaceutical preparations containing at least one compound of the formula I and / or one of its physiologically acceptable salts and / or solvates for the treatment or prophylaxis of diseases which are influenced by the binding of the compounds of the formula I to 5 HT receptors ,
Diese Zubereitungen können als Arzneimittel in der Human- oderThese preparations can be used as medicinal products in human or
Veterinärmedizin verwendet werden. Als Trägerstoffe kommen organische oder anorganische Substanzen in Frage, die sich für die enterale (z.B. orale), parenterale oder topische Applikation eignen und mit den neuen Verbindungen nicht reagieren, beispielsweise Wasser, pflanzliche Öle, Benzylalkohole, Alkylenglykole, Polyethylenglykole, Glycerintriacetat,Veterinary medicine can be used. Suitable carriers are organic or inorganic substances which are suitable for enteral (e.g. oral), parenteral or topical application and do not react with the new compounds, for example water, vegetable oils, benzyl alcohols, alkylene glycols, polyethylene glycols, glycerol triacetate,
Gelatine, Kohlenhydrate wie Lactose oder Stärke, Magnesiumstearat, Talk, Vaseline. Zur oralen Anwendung dienen insbesondere Tabletten, Pillen, Dragees, Kapseln, Pulver, Granulate, Sirupe, Säfte oder Tropfen, zur rektalen Anwendung Suppositorien, zur parenteralen Anwendung Lösun- gen, vorzugsweise ölige oder wässrige Lösungen, ferner Suspensionen,Gelatin, carbohydrates such as lactose or starch, magnesium stearate, talc, petroleum jelly. Tablets, pills, dragees, capsules, powders, granules, syrups, juices or drops are used for oral use, suppositories for rectal use, solutions, preferably oily or aqueous solutions, and suspensions for parenteral use.
Emulsionen oder Implantate, für die topische Anwendung Salben, Cremes oder Puder. Die neuen Verbindungen können auch lyophilisiert und die erhaltenen Lyophilisate z.B. zur Herstellung von Injektionspräparaten verwendet werden. Die angegebenen Zubereitungen können sterilisiert sein und/oder Hilfsstoffe wie Gleit-, Konservierungs-, Stabilisierungsund/oder Netzmittel, Emulgatoren, Salze zur Beeinflussung des osmo- tischen Druckes, Puffersubstanzen, Färb-, Geschmacks- und /oder ein oder mehrere weitere Wirkstoffe enthalten, z.B. ein oder mehrere Vitamine.Emulsions or implants, for topical application of ointments, creams or powders. The new compounds can also be lyophilized and the lyophilizates obtained e.g. can be used for the production of injectables. The specified preparations can be sterilized and / or contain auxiliaries such as lubricants, preservatives, stabilizers and / or wetting agents, emulsifiers, salts for influencing the osmotic pressure, buffer substances, coloring, flavoring and / or one or more further active ingredients, eg one or more vitamins.
Dabei werden die erfindungsgemäßen Substanzen in der Regel vorzugsweise in Dosierungen zwischen 1 und 500 mg, insbesondere zwischen 5 und 100 mg pro Dosierungseinheit verabreicht. Die tägliche Dosierung liegt vorzugsweise zwischen etwa 0,02 und 10 mg/kg Körpergewicht. Die spezielle Dosis für jeden Patienten hängt jedoch von den verschiedensten Faktoren ab, beispielsweise von der Wirksamkeit der eingesetzten speziellen Verbindung, vom Alter, Körpergewicht, allgemeinen Gesundheitszustand, Geschlecht, von der Kost, vom Verabreichungszeitpunkt und -weg, von der Ausscheidungsgeschwindigkeit, Arzneistoffkombination und Schwere der jeweiligen Erkrankung, welcher die Therapie gilt. Die orale Applikation ist bevorzugt.The substances according to the invention are generally preferably administered in doses between 1 and 500 mg, in particular between 5 and 100 mg, per dosage unit. The daily dosage is preferably between about 0.02 and 10 mg / kg body weight. However, the specific dose for each patient depends on a wide variety of factors, for example on the effectiveness of the particular compound used, on age, body weight, in general Health status, gender, the diet, the time and route of administration, the rate of excretion, the combination of drugs and the severity of the disease to which the therapy applies. Oral application is preferred.
Bevorzugte Verbindungen der Formel I weisen nanomolare Affinität zu den 5 HT2A-Rezeptoren auf, mit teilweise geringer Affinität zum 5 HT2C- Rezeptor.Preferred compounds of the formula I have nanomolar affinity for the 5 HT2A receptors, some with low affinity for the 5 HT2C receptor.
Vor- und nachstehend sind alle Temperaturen in °C angegeben. In den nachfolgenden Beispielen bedeutet "übliche Aufarbeitung": Man gibt, falls erforderlich, Wasser hinzu, extrahiert mit Ethylacetat oder Dichlormethan, trennt ab, trocknet die organische Phase über Natriumsulfat, dampft ein und reinigt durch Chromatographie an Kieselgel und /oder durch Kristallisation.All temperatures above and below are given in ° C. In the following examples, "customary work-up" means: if necessary, water is added, extracted with ethyl acetate or dichloromethane, the mixture is separated off, the organic phase is dried over sodium sulfate, evaporated and purified by chromatography on silica gel and / or by crystallization.
Beispiel 1example 1
Eine Lösung von 6,218 g 1 und 1,360 g Tetrakis(triphenylphosphin)- palladium(O) in 200 ml Ethylenglykoldimethyl-ether wird leicht erwärmt und nach Zugabe von 5,26 g 2 und 13,107 g Cäsiumfluorid für 6 Std. unter Rückfluß erhitzt. Durch übliche Aufarbeitung der Reaktionsmischung erhält man 3.A solution of 6.218 g of 1 and 1.360 g of tetrakis (triphenylphosphine) palladium (O) in 200 ml of ethylene glycol dimethyl ether is warmed slightly and after the addition of 5.26 g of 2 and 13.107 g of cesium fluoride is heated under reflux for 6 hours. Working up the reaction mixture in a customary manner gives 3.
Beispiel 2Example 2
4 3,02 g 3 werden in Gegenwart von 1 ,50 g Raney-Nickel in 160 ml Methanol bei normalem Druck hydriert. Durch übliche Aufarbeitung erhält man 4.4 3.02 g 3 are hydrogenated in the presence of 1.50 g of Raney nickel in 160 ml of methanol at normal pressure. The usual work-up gives 4.
Beispiel 3Example 3
ClCl
2,34 g 4 werden in 23,3 ml Wasser gegeben und unter Rühren bei -5°C bis 0°C innerhalb von 15 min. tropfenweise mit 43,1 ml 32%iger wässriger Salzsäure versetzt. Anschließend wird eine Lösung von 0,949 g Natriumnitrit in 11 ,4 ml Wasser innerhalb von 20 min. zugetropft für weitere 30 min. gerührt. Die erhaltene Mischung tropft man bei -5°C bis 0°C innerhalb von 20 min. in eine Lösung aus 15,58 g Zinn(ll)chlorid-Dihydrat und 35,3 ml konzentrierter Salzsäure. Das Lösungsmittel wird entfernt und der Rückstand wie üblich aufgearbeitet, wodurch 5 erhalten wird.2.34 g of 4 are placed in 23.3 ml of water and with stirring at -5 ° C to 0 ° C within 15 min. 43.1 ml of 32% aqueous hydrochloric acid are added dropwise. Then a solution of 0.949 g of sodium nitrite in 11.4 ml of water within 20 min. added dropwise for a further 30 min. touched. The mixture obtained is added dropwise at -5 ° C to 0 ° C within 20 min. in a solution of 15.58 g of tin (II) chloride dihydrate and 35.3 ml of concentrated hydrochloric acid. The solvent is removed and the residue is worked up as usual to give 5.
Beispiel 4Example 4
88th
Eine Lösung von 41 ,00 ml 6 und 61 ,97 ml 7 in 820 ml Tetrahydrofuran wird für 80 Stunden gerührt und anschließend destilliert, wodurch 8 erhalten wird (Kp.161°C bei 0,4 mbar). Beispiel 5A solution of 41, 00 ml 6 and 61, 97 ml 7 in 820 ml tetrahydrofuran is stirred for 80 hours and then distilled, whereby 8 is obtained (bp. 161 ° C at 0.4 mbar). Example 5
8 48 4
3,95 g 8, 3,30 g 4 und 170 ml Ethanol werden zusammengegeben und für 5 Stunden unter Rückfluß erhitzt. Durch übliche Aufarbeitung der Reaktionsmischung wird 9 erhalten.3.95 g 8, 3.30 g 4 and 170 ml ethanol are combined and heated under reflux for 5 hours. 9 is obtained by customary working up of the reaction mixture.
Beispiel eExample e
1010
Zu einer Suspension von 1,139 g Lithiumaluminiumhydrid in 25 ml Tetrahydrofuran wird unter Rühren und Eiskühlung unter Stickstoffatmosphäre eine Lösung von 2,090 g 9 in 25 ml THF getropft. Nach 1 h Rühren werden weitere 0,500 g Lithiumaluminiumhydrid zugefügt. Nach weiteren 2 h Rühren wird unter Eiskühlung gesättigte Natriumchlorid-Iösung zugetropft und die Mischung wie üblich aufgearbeitet, wodurch 10 erhalten wird.A solution of 2.090 g 9 in 25 ml THF is added dropwise to a suspension of 1.139 g lithium aluminum hydride in 25 ml tetrahydrofuran with stirring and ice cooling under a nitrogen atmosphere. After stirring for 1 h, a further 0.500 g of lithium aluminum hydride are added. After stirring for a further 2 h, saturated sodium chloride solution is added dropwise while cooling with ice and the mixture is worked up in the customary manner, giving 10.
Beispiel 7 Example 7
1111
1,480 g 10, 2,897 g Mangan(IV)oxid, 9,00 ml Tetrahydrofuran und 3,0 ml Dichlormethan werden zusammengegeben und für 3 Tage gerührt. Nach Filtration entfernt man das Lösungsmitte! und arbeitet den Rückstand wie üblich auf, wodurch 11 erhalten wird.1.480 g 10, 2.897 g manganese (IV) oxide, 9.00 ml tetrahydrofuran and 3.0 ml dichloromethane are combined and stirred for 3 days. After filtration, the solvent is removed! and work up the residue as usual to give 11.
Beispiel 8Example 8
11 12 1311 12 13
Eine Lösung von 0,103 g 11 und 0,040 ml 12 in 2,00 ml Dichlorethan und 1,00 ml Tetrahydrofuran wird mit 0,017 ml Essigsäure versetzt und für 3 Stunden gerührt. Nach Zugabe von 0,120 g Natriumtriacetoxyborhydrid wird die Mischung über Nacht gerührt, anschließend mit gesättigter Natriumhydrogencarbonat versetzt und wie üblich aufgearbeitet, wodurch 13 erhalten wird. eispiel 9A solution of 0.103 g 11 and 0.040 ml 12 in 2.00 ml dichloroethane and 1.00 ml tetrahydrofuran is mixed with 0.017 ml acetic acid and stirred for 3 hours. After adding 0.120 g of sodium triacetoxyborohydride, the mixture is stirred overnight, then saturated sodium bicarbonate is added and the mixture is worked up in the customary manner, giving 13. example 9
Cl ClCl Cl
14 15 1614 15 16
Zu einer Lösung von 91,30 mg 14, 46,00 mg 15 und 6,500 mg Bisdichloropalladium(ll) in 3,00 ml Dimethoxyethan wird 1,00 ml einer 2M Natriumcarbonatlösung getropft. Die Mischung wird über Nacht unter Rückfluss erhitzt. Der Ansatz wird nach Abkühlen mit 5 ml Wasser versetzt und wie üblich aufgearbeitet, wodurch 16 erhalten wird.1.00 ml of a 2M sodium carbonate solution is added dropwise to a solution of 91.30 mg 14, 46.00 mg 15 and 6.500 mg bisdichloropalladium (II) in 3.00 ml of dimethoxyethane. The mixture is refluxed overnight. After cooling, the mixture is mixed with 5 ml of water and worked up as usual, giving 16.
Beispiel 10Example 10
17 18 1917 18 19
Zu einer Lösung von 0,685 g 17 und 0,789 g 218 in 10 ml THF wird unter Rühren und Eiskühlung eine Lösung von 0,258 g Kalium-tert-butylat in 5 ml THF bei max. 7°C getropft. Die Reaktionsmischung wird für 2 Tage gerührt und anschließend wie üblich aufgearbeitet, wodurch 19 erhalten wird. Beispiel 11A solution of 0.258 g of potassium tert-butoxide in 5 ml of THF is added to a solution of 0.685 g of 17 and 0.789 g of 218 in 10 ml of THF with stirring and ice-cooling at max. Dropped 7 ° C. The reaction mixture is stirred for 2 days and then worked up as usual to give 19. Example 11
20 2120 21
Eine Mischung von 50,00 mg 20, 3,00 ml einer 16%igen wässrigenA mixture of 50.00 mg 20, 3.00 ml of a 16% aqueous
Schwefelsäure und 3,00 ml Toluol wird für 2 Stunden unter Rückfluß erhitzt. Anschließend läßt man die Mischung für 3 Tage bei Raumtemperatur rühren. Durch übliche Aufarbeitung erhält man 21.Sulfuric acid and 3.00 ml of toluene are heated under reflux for 2 hours. The mixture is then left to stir at room temperature for 3 days. The usual work-up gives 21.
Beispiel 12Example 12
21 12 22 Zu einer Lösung von 61 ,000 mg 21 und 22,35 mg Morpholin in 3,000 ml Dichlorethan und 1,5 ml Tetrahydrofuran werden 0,010 ml Essigsäure gegeben. Die Mischung wird für 3 h gerührt und anschließend mit 68,668 mg iMatriumtriacetoxyborhydrid versetzt. Nach 2 tägigem Rühren wird wie üblich aufgearbeitet, wodurch die freie Base von 22 erhalten wird. Nach Umsetzung der Base mit einem Equivalent einer 0,1 M HCI/2-Propanol- Lösung fällt das Hydrochlorid 22 durch Zugabe von Methyl-tert-Butylether aus, so daß es durch Filtration gewonnen werden kann.21 12 22 0.010 ml of acetic acid are added to a solution of 61,000 mg of 21 and 22.35 mg of morpholine in 3.000 ml of dichloroethane and 1.5 ml of tetrahydrofuran. The mixture is stirred for 3 h and then 68.668 mg of sodium triacetoxyborohydride are added. After stirring for 2 days, the mixture is worked up in the customary manner, giving the free base of 22. After the base has been reacted with an equivalent of a 0.1 M HCl / 2-propanol solution, the hydrochloride 22 precipitates by adding methyl tert-butyl ether, so that it can be obtained by filtration.
Beispiel 13Example 13
17 23 2417 23 24
Zu einer Lösung von 200,00 mg 17 und 74,66 mg o-To a solution of 200.00 mg 17 and 74.66 mg o-
Methylhydroxylaminhydrochlorid 23 in 8,50 ml Dichlorethan und 4,5 ml Tetrahydrofuran werden 0,033 ml Essigsäure gegeben und 3 h gerührt. Die Mischung wird für 3 h gerührt und anschließend mit 130,287 mg Natriumtriacetoxyborhydrid versetzt. Nach 5 stündigem Rühren wird wie üblich aufgearbeitet, wodurch 24 erhalten wird. Methyl hydroxylamine hydrochloride 23 in 8.50 ml dichloroethane and 4.5 ml tetrahydrofuran are added 0.033 ml acetic acid and stirred for 3 hours. The mixture is stirred for 3 h and then 130.287 mg of sodium triacetoxyborohydride are added. After stirring for 5 hours, the mixture is worked up in the customary manner, giving 24.
0,160 g 17 und 0,087 ml 25 werden in einer Mischung aus 3,00 ml Dichlorethan und 1,50 ml Tetrahydrofuran mit 0,026 ml Essigsäure versetzt und für 3 Stunden gerührt. Nach Zugabe von 0,188 g 26 wird über Nacht weiter gerührt und wie üblich aufgearbeitet, wodurch 28, die freie Base von 27, erhalten wird. Durch Umsetzung mit 1 Equivalent einer 0,1 M Lösung von HCI in 2-Propanol kann das Hydrochlorid 27 erhalten werden.0.160 g 17 and 0.087 ml 25 are mixed in a mixture of 3.00 ml dichloroethane and 1.50 ml tetrahydrofuran with 0.026 ml acetic acid and stirred for 3 hours. After the addition of 0.188 g of 26, the mixture is stirred overnight and worked up as usual, whereby 28, the free base of 27, is obtained. The hydrochloride 27 can be obtained by reaction with 1 equivalent of a 0.1 M solution of HCl in 2-propanol.
Beispiel 15Example 15
28 2928 29
80,00 mg 28 werden in Gegenwart von 0,70 g Raney-Nickel in 10 ml Ethanol bei normalem Druck hydriert. Durch übliche Aufarbeitung und80.00 mg 28 are hydrogenated in the presence of 0.70 g Raney nickel in 10 ml ethanol under normal pressure. Through usual workup and
Zugabe von Salzsäure erhält man 29. Beispiel 16Addition of hydrochloric acid gives 29. Example 16
3131
1 ,20 g 6, 2,70 g 30, 6,0 ml Salzsäure und 40,0 ml Dimethylacetamid werden zusammengegeben und über Nacht gerührt. Nach Zugabe von 40 ml Wasser wird die Mischung für weitere 4 h gerührt und wie üblich aufgearbeitet, wodurch 31 erhalten wird.1, 20 g 6, 2.70 g 30, 6.0 ml hydrochloric acid and 40.0 ml dimethylacetamide are combined and stirred overnight. After adding 40 ml of water, the mixture is stirred for a further 4 h and worked up as usual, giving 31.
Beispiel 17Example 17
31 3231 32
Zu einer Lösung von 1 ,00 g 31 und 630,0 mg 2 in 15,0 mlTo a solution of 1.00 g 31 and 630.0 mg 2 in 15.0 ml
Ethylenglycoldimethylether werden 4,00 ml einer wässrigen 2M Natriumcarbonat-Lösung und 150,00 mg Tetrakis(triphenylphosphin)- palladium(O) gegeben. Die Mischung wird für 3 Stunden unter Rückfluß erhitzt. Nach dem Abkühlen wird das Gemisch wie üblich aufgearbeitet, wodurch 32 erhalten wird. Ethylene glycol dimethyl ether is given 4.00 ml of an aqueous 2M sodium carbonate solution and 150.00 mg of tetrakis (triphenylphosphine) palladium (O). The mixture is refluxed for 3 hours. After cooling, the mixture is worked up as usual, giving 32.
32 3332 33
Zu einer Suspension von 450,00 mg Lithiumaluminiumhydrid in 20 ml Tetrahydrofuran wird in einer Stickstoffatmosphäre eine Lösung von 3,6 g 32 in 30 ml Tetrahydrofuran getropft Die Mischung wird für 2 Stunden gerührt. Unter Eiskühlung werden langsam 50 ml einer Mischung von Wasser und Tetrahydrofuran (1:1 v/v) zugetropft, der entstandene Niederschlag wird abgesaugt und das Filtrat wie üblich aufgearbeitet, wodurch 33 erhalten wird.A solution of 3.6 g of 32 in 30 ml of tetrahydrofuran is added dropwise to a suspension of 450.00 mg of lithium aluminum hydride in 20 ml of tetrahydrofuran in a nitrogen atmosphere. The mixture is stirred for 2 hours. While cooling with ice, 50 ml of a mixture of water and tetrahydrofuran (1: 1 v / v) are slowly added dropwise, the precipitate formed is filtered off with suction and the filtrate is worked up in the customary manner, giving 33.
33 3433 34
1 ,600 g 33, 4,00 g Mangan(IV)-oxid und 50,00 ml Dichlormethan werden ∑usammengegeben und bei 4 Stunden bei Raumtemperatur gerührt. Nach Zugabe von weiteren 2 g Mangan(IV)-oxid wird für 2 Tage gerührt und anschließend wie üblich aufgearbeitet, wodurch 34 erhalten wird.1,600 g 33, 4.00 g manganese (IV) oxide and 50.00 ml dichloromethane are combined and stirred at room temperature for 4 hours. To Addition of a further 2 g of manganese (IV) oxide is stirred for 2 days and then worked up as usual, giving 34.
Beispiel 20Example 20
34 35 3634 35 36
Zu einer Lösung von 430,00 mg 34 und 0,210 ml 35 in 10,0 ml Dichlorethan und 5,0 ml Tetrahydrofuran wird 0,10 ml Essigsäure gegeben. Die Raktionsmischung wird für 3 Stunden gerührt. Anschließend werden 0,50 g Natriumtriacetoborhydrid zugefügt, die Mischung für 2 Stunden gerührt und danach wie üblich aufgearbeitet, wodurch die freie Base von 36 erhalten wird, aus der durch Zugabe von etherischer HCI 36 in kristalliner Form erhalten wird (Fp.:277°C).0.10 ml of acetic acid is added to a solution of 430.00 mg of 34 and 0.210 ml of 35 in 10.0 ml of dichloroethane and 5.0 ml of tetrahydrofuran. The raction mixture is stirred for 3 hours. Then 0.50 g of sodium triacetoborohydride are added, the mixture is stirred for 2 hours and then worked up as usual, whereby the free base of 36 is obtained, from which 36 is obtained in crystalline form by addition of ethereal HCl (mp: 277 ° C. ).
Analog werden unter Verwendung der entsprechenden Vorstufen die folgenden Verbindungen für die erfindungsgemäße Verwendung erhalten:The following compounds for the use according to the invention are obtained analogously using the corresponding precursors:
Beispiele 21 - 240:Examples 21-240:
IC50 [mol/L]IC50 [mol / L]
"(21) [1 -Biphenyl-4-yl-5-(2-f luoro-ρhenyl)-1 H-pyrazol-4-yl]- 1.20E-06 methanol " (21) [1-biphenyl-4-yl-5- (2-f luoro-ρhenyl) -1 H-pyrazol-4-yl] - 1.20E-06 methanol
(22) 1-biρhenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1.40E-06 ylmethyl-acetate(22) 1-Biρhenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1.40E-06 ylmethyl acetate
(23) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 3,00E-08 ylmethylj-piperidin (24) 1-Benzyl-4-[1-biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H- 1 ,70E-07 pyrazol-4-ylmethyl]-piperazin(23) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 3.00E-08 ylmethylj-piperidine (24) 1-Benzyl-4- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-1, 70E-07 pyrazol-4-ylmethyl] piperazine
(25) 4-{1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 5.60E-07 ylmethyl]-piperidin-4-yl}-morpholin(25) 4- {1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 5.60E-07 ylmethyl] piperidin-4-yl} morpholine
(26) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 3,40E-08 ylmethyl]-(3-methoxy-propy!)-amin(26) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 3.40E-08 ylmethyl] - (3-methoxy-propy!) - amine
(27) 2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.80E-07 ylmethyl]-1 ,3,4,6,7, 11 b-hexahydro-2H-pyrazino[2,1- ajisoquinolin(27) 2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.80E-07 ylmethyl] -1, 3,4,6,7, 11 b -hexahydro-2H-pyrazino [2,1-ajisoquinoline
(28) 4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1 ,10E-06 ylmethylj-morpholin(28) 4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1, 10E-06 ylmethylj-morpholine
(29) {[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,70E-06 ylmethyl]-amino}-essigsäure (30) 1-Biphenyl-4-yl-4-(2,5-dihydro-pyrrol-1-ylmethyl)-5-(2- 3.60E-08 fluoro-phenyl)-1 H-pyrazole(29) {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 70E-06 ylmethyl] amino} acetic acid (30) 1-biphenyl-4 -yl-4- (2,5-dihydro-pyrrol-1-ylmethyl) -5- (2-3.60E-08 fluoro-phenyl) -1 H-pyrazole
(31) 1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4.80E-08 ylmethylj-azepan (32) Benzyl-[1-biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol- 3.20E-07(31) 1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4.80E-08 ylmethylj-azepane (32) benzyl- [1-biphenyl-4- yl-5- (2-fluoro-phenyl) -1 H-pyrazole-3.20E-07
4-ylmethyl]-ethyl-amin4-ylmethyl] -ethyl-amine
(33) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 5.50E-08 ylmethyl]-diethyl-amin(33) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 5.50E-08 ylmethyl] diethylamine
(34) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 2.10E-08 ylmethyl]-dimethyl-amin(34) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4-2.10E-08 ylmethyl] dimethyl amine
(35) 1 -Biphenyl-4-yl-5-(2-f luoro-phenyl)-4-pyrrolidin-1 - 3.20E-08 ylmethyl-1 H-pyrazole(35) 1-biphenyl-4-yl-5- (2-f luorophenyl) -4-pyrrolidin-1 - 3.20E-08 ylmethyl-1 H-pyrazole
(36) 2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 7,OOE-08 ylmethyl]-1 ,2,3,4-tetrahydro-isoquinolin(36) 2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 7, OOE-08 ylmethyl] -1, 2,3,4-tetrahydro-isoquinoline
(37) {1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.00E-07 ylmethyl]-piperidin-4-yl}-dimethyl-amin(37) {1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-2.00E-07 ylmethyl] piperidin-4-yl} dimethylamine
(38) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1.70E-07 ylmethyl]-1 ,2,3,6-tetrahydro-pyridin(38) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1.70E-07 ylmethyl] -1, 2,3,6-tetrahydro-pyridine
(39) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1 ,60E-07 ylmethyl]-methyl-(1-methyl-piρeridin-4-yI)-amin(39) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1, 60E-07 ylmethyl] -methyl- (1-methyl-piρeridin-4-yl) -amine
40) [1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,40E-08 ylmethylj-(4-methyI-piperazin-1-yl)-amin40) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1,40E-08 ylmethylj- (4-methyl-piperazin-1-yl) amine
41) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.40E-08 ylmethylj-4-methyl-piperazin41) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.40E-08 ylmethylj-4-methyl-piperazine
42) 4-{2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,20E-08 yl]-ethyl}-morpholin42) 4- {2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 20E-08 yl] ethyl} morpholine
43) 1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-3- 1 ,20E-07 ylmethylj-piperidin43) 1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-3- 1, 20E-07 ylmethylj-piperidine
44) 4-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-3- 1 , 10E-06 ylmethylj-morpholin44) 4- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-3- 1, 10E-06 ylmethylj-morpholine
(45) 1-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-3- 3.00E-07 ylmethyl]-4-methyl-piperazin(45) 1- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-3- 3.00E-07 ylmethyl] -4-methyl-piperazine
(46) 4-{3-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,70E-08 yl]-allyl}-morpholin(46) 4- {3- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 70E-08 yl] allyl} morpholine
(47) 4-{3-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2,30E-08 yl]-propylj-morpholin(47) 4- {3- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.30E-08 yl] propylj-morpholine
(48) 1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-4-(2- 5,10E-07 methoxymethyl-pyrrolidin-1 -ylmethyl)-1 H-pyrazole(48) 1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -4- (2- 5,10E-07 methoxymethyl-pyrrolidin-1-ylmethyl) -1 H-pyrazole
(49) 1-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,30E-07 ylmethyl]-4-methyl-piperidin (50) N-{1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2,90E-08 ylmethyl]-pyrrolidin-3-yl}-acetamid(49) 1- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 30E-07 ylmethyl] -4-methyl-piperidine (50) N- { 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.90E-08 ylmethyl] pyrrolidin-3-yl} acetamide
(51 ) {1 -[1 -Biphenyl-4-yi-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.70E-07 ylmethyl]-piperidin-2-ylmethyl}-diethyl-amin (52) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl]- 8,20E-07(51) {1 - [1 -Biphenyl-4-yi-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.70E-07 ylmethyl] piperidin-2-ylmethyl} diethylamine ( 52) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl] - 8.20E-07
1 -(4-methyl-piperazin-1 -yl)-methanon1 - (4-methyl-piperazin-1-yl) methanone
(53) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1 ,40E-08 ylmethyl]-pyrrolidin-3-ol(53) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1,40E-08 ylmethyl] pyrrolidin-3-ol
(54) 4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 8.20E-08 ylmethyl]-piperazin-1-carboxylsäure tert-butyl ester (55) 1 -[1 -Biphenyl-4-yI-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2,60E-08 ylmethylj-piperazin(54) 4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 8.20E-08 ylmethyl] piperazine-1-carboxylic acid tert-butyl ester (55) 1 - [1 -Biphenyl-4-yI-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.60E-08 ylmethylj-piperazine
(56) 1-[5-(2-Fluoro-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- 1 ,50E-07 pyra∑o!-4-yImβthyl3-piperazin (57) 1-[5-(2-Fluoro-phenyl)-1-(6-phenyl-pyridin-3-yl)-1H- 2.20E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin(56) 1- [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H- 1, 50E-07 pyra∑o! -4-yImβthyl3-piperazine (57 ) 1- [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1H-2.20E-07 pyrazol-4-ylmethyl] -4-methyl-piperazine
(58) 1-(1-Biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4- 5.00E-08 ylmethyl)-4-methyl-pipera∑in (59) 4-(1-Biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4- 7.80E-07 ylmethyl)-piperazin-1 -carboxylsäure tert-butylester(58) 1- (1-biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4- 5.00E-08 ylmethyl) -4-methyl-pipera∑in (59) 4- (1- Biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4- 7.80E-07 ylmethyl) -piperazin-1-carboxylic acid tert-butyl ester
(60) 1-(1-Biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4- 2.00E-07 ylmethyl)-piperazin(60) 1- (1-Biphenyl-4-yl-5-pyridin-2-yl-1H-pyrazol-4-2.00E-07 ylmethyl) piperazine
(61) 4-[1-(4*-Fluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl)-1 H- 5.20E-07 pyrazol-4-ylmethyl]-morpholin(61) 4- [1- (4 * -Fluorobiphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- 5.20E-07 pyrazol-4-ylmethyl] morpholine
(62) 4-[5-(2-Fluoro-phenyl)-1-(4-thiophen-2-yl-pheήyl)-1 H- 6.20E-07 pyrazol-4-ylmethyl]-morphoIin(62) 4- [5- (2-Fluoro-phenyl) -1- (4-thiophene-2-yl-phenyl) -1 H-6.20E-07 pyrazol-4-ylmethyl] morpholine
(63) 1-[1-(2'-Fluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl)-1 H- 9,30E-08 pyrazol-4-ylmethyI]-4-methyl-piperazin(63) 1- [1- (2'-Fluoro-biphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- 9.30E-08 pyrazol-4-ylmethyI] -4-methyl- piperazine
(64) 1-[1-(4'-Fluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl)-1 H- 7,80E-09 pyrazol-4-ylmethyl]-4-methyl-piperazin(64) 1- [1- (4'-fluoro-biphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- 7.80E-09 pyrazol-4-ylmethyl] -4-methyl- piperazine
(65) 1-[1-(2\5'-Difluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl> 5.50E-08 1H-pyrazol-4-ylmethyl]-4-methyl-piperazin(65) 1- [1- (2 \ 5'-Difluorobiphenyl-4-yl) -5- (2-fluoro-phenyl> 5.50E-08 1H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(66) 1 -[5-(2-Fluoro-phenyl)-1 -(4-thiophen-3-yl-phenyl)-1 H- 1 ,40E-08 pyrazol-4-ylmethyl]-4-methyl-piperazin(66) 1 - [5- (2-Fluoro-phenyl) -1 - (4-thiophene-3-yl-phenyl) -1 H-1,40E-08 pyrazol-4-ylmethyl] -4-methyl-piperazine
(67) 1-(Biphenyl-4-yl-trifluoromethyl-1 H-pyrazol-4-ylmethyl)- 2.60E-07 4-methyl-piperazin(67) 1- (Biphenyl-4-yl-trifluoromethyl-1 H-pyrazol-4-ylmethyl) - 2.60E-07 4-methyl-piperazine
(68) 1-[1-(2',5*-Difluoro-biphenyl-4-yl)-5-phenyl-1 H-pyrazol- 1 ,10E-07 4-ylmethyl]-4-methyl-piperazin(68) 1- [1- (2 ', 5 * -Difluorobiphenyl-4-yl) -5-phenyl-1H-pyrazole-1, 10E-07 4-ylmethyl] -4-methyl-piperazine
(69) 1-[1-(2',5,-Difluoro-biphenyl-4-yl)-5-furan-2-yl-1 H- 3.60E-08 pyrazol-4-ylmethyl]-4-methyl-pipera∑in (70) 1-[5-Furan-2-yI-1-(4-thiophen-3-yl-phenyl)-1 H-pyrazol- 4.50E-09(69) 1- [1- (2 ', 5 , -Difluorobiphenyl-4-yl) -5-furan-2-yl-1 H-3.60E-08 pyrazol-4-ylmethyl] -4-methyl- pipera∑in (70) 1- [5-furan-2-yI-1- (4-thiophene-3-yl-phenyl) -1 H-pyrazole-4.50E-09
4-yImethyl]-4-methyl-piperazin (71 ) 1 -[1 -(2',5'-Difluoro-biphenyl-4-yl)-5-(2-methoxy-phenyl)- 7.70E-08 1H-pyrazol-4-ylmethyl]-4-methyl-piperazin4-yImethyl] -4-methyl-piperazine (71) 1 - [1 - (2 ', 5'-Difluorobiphenyl-4-yl) -5- (2-methoxyphenyl) - 7.70E-08 1H-pyrazol-4-ylmethyl] -4-methyl piperazine
(72) 4-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyra∑ol-4- 5,80E-07 ylmethyl]-amino}-piperidin-1 -carboxylsäureethyl ester(72) 4 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyra∑ol-4- 5.80E-07 ylmethyl] amino} piperidine-1-carboxylic acid ethyl ester
(73) {4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.90E-07 ylmethyl]-piperazin-1-yl}-essisäure ethyl ester(73) {4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.90E-07 ylmethyl] piperazin-1-yl} -essic acid ethyl ester
(74) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4J0E-07 ylmethyl3-piperidin-4-yl-amin(74) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4J0E-07 ylmethyl3-piperidin-4-yl-amine
(75) {4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.30E-07 ylmethyl]-piperazin-1 -yl}-(75) {4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.30E-07 ylmethyl] piperazin-1 -yl} -
(76) N1-[1-Biphenyl-4-yI-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.50E-09 ylmethyl]-ethan-1 ,2-diamin (77) 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 5,20E-09 ylmethyl]-amino}-ethanol(76) N 1 - [1-Biphenyl-4-yI-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.50E-09 ylmethyl] ethane-1,2-diamine (77) 2 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 5.20E-09 ylmethyl] amino} ethanol
(78) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,60E-08 ylmethyl]-(2-methoxy-ethyl)-amin (79) 2-{4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 2.80E-07 ylmethyl]-piperazin-1-yl}-ethanol(78) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 60E-08 ylmethyl] - (2-methoxyethyl) amine (79) 2 - {4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 2.80E-07 ylmethyl] piperazin-1-yl} ethanol
(80) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2,80E-07 ylmethyl]-4-ethyl-piperidin-4-ol(80) 1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.80E-07 ylmethyl] -4-ethyl-piperidin-4-ol
(81 ) 1 -[1 -Biphenyl-4- l-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4.30E-07 ylmethyl]-piperidin-4-ol(81) 1 - [1 -Biphenyl-4- l-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4.30E-07 ylmethyl] piperidin-4-ol
(82) 5-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,60E-07 ylmethyl]-2-oxa-5-aza-bicyclo[2.2.1 Jheptan(82) 5- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 60E-07 ylmethyl] -2-oxa-5-aza-bicyclo [2.2 .1 Jheptan
(83) 8-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1 ,10E-06 ylmethyl]-8-aza-bicyclo[3.2.1]octan-3-ol(83) 8- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1, 10E-06 ylmethyl] -8-aza-bicyclo [3.2.1] octane 3-ol
(84) 4-[5-(2-Fluoro-phenyl)-1 -(4-trifluoromethyl-phenyl)-1 H- 8,00E-09 pyrazol-4-ylmethyl]-piperazin-1 -carboxylicacid tert-butyl ester(84) 4- [5- (2-Fluoro-phenyl) -1 - (4-trifluoromethylphenyl) -1 H- 8.00E-09 pyrazol-4-ylmethyl] piperazin-1-carboxylic acid tert-butyl ester
(85) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 8,70E-07 ylmethyl]-piperidin-4-carboxylsäure amid 86) 1-[5-(2-Fluoro-phenyl)-1 -(4-trif luoromethyl-phenyl)-1 H- 4.30E-08 pyrazol-4-ylmethyI]-piperazin(85) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 8.70E-07 ylmethyl] piperidine-4-carboxylic acid amide 86) 1- [5- (2-Fluoro-phenyl) -1 - (4-trifluoromethyl-phenyl) -1 H- 4.30E-08 pyrazol-4-ylmethyl] piperazine
87) 1-[5-(2-Fluoro-phenyl)-1 -(4-trif luoromethyl-phenyl)-1 H- 1 ,60E-07 pyra∑ol-4-ylmethyl]-4-rnethyl-pipera∑in87) 1- [5- (2-Fluoro-phenyl) -1 - (4-trifluoromethyl-phenyl) -1 H-1, 60E-07 pyra∑ol-4-ylmethyl] -4-methyl piperain
88) [1-Biphenyl-4-yl-5-(2-fluoro-phenyI)-1H-pyra∑ol-4- 2,00E-08 ylmethyl]-(1-ethyl-pyrrolidin-2-yImβthyl)-amin88) [1-Biphenyl-4-yl-5- (2-fluoro-phenyI) -1H-pyra∑ol-4-2.00E-08 ylmethyl] - (1-ethyl-pyrrolidin-2-yImβthyl) amine
89) [1-Biphenyl-4- l-5-(2-fluoro-phenyl)-1H-pyra∑ol-4- 1,80E-07 ylmethyl]-pyridin-3-ylmethyl-amin89) [1-Biphenyl-4- l-5- (2-fluoro-phenyl) -1H-pyra∑ol-4- 1.80E-07 ylmethyl] pyridin-3-ylmethyl-amine
90) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.80E-08 ylmethyl]-4-ethyl-piperazin90) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.80E-08 ylmethyl] -4-ethyl-piperazine
91) 2-{4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 3,70E-08 ylmethyl]-piperazin-1-yl}-1-pyrrolidin-1-yl-ethanon91) 2- {4- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 3.70E-08 ylmethyl] -piperazin-1-yl} -1- pyrrolidin-1-yl-ethanone
(92) 2-{[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,60E-08 ylmethyl]-methyl-amino}-ethanol(92) 2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 60E-08 ylmethyl] methylamino} ethanol
(93) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.40E-09 yImethyl]-4-methyl-[1,4]diazepam(93) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.40E-09 yImethyl] -4-methyl- [1,4] diazepam
(94) 8-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4.00E-07 ylmethylj-1-phenyl-1 ,3,8-triaza-spiro[4.5]decän-4-on(94) 8- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4.00E-07 ylmethylj-1-phenyl-1, 3,8-triaza-spiro [4.5] DECAEN-4-one
(95) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,00E-07 ylmethyl]-3,5-dimethyl-piperazin(95) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1,00E-07 ylmethyl] -3,5-dimethyl-piperazine
(96) 1 -[1 -(2*-Fluoro-biphenyl-4-yl)-5-phenyl-1 H-pyrazol-4- 8.20E-07 ylmethyl]-4-methyl-piperazin(96) 1 - [1 - (2 * -Fluorobiphenyl-4-yl) -5-phenyl-1H-pyrazol-4- 8.20E-07 ylmethyl] -4-methyl-piperazine
(97) 1-[1-(4'-Fluoro-biphenyl-4-yl)-5-phenyl-1 H-pyrazol-4- 1.30E-08 ylmethyl]-4-methyl-piperazin(97) 1- [1- (4'-Fluoro-biphenyl-4-yl) -5-phenyl-1H-pyrazol-4- 1.30E-08 ylmethyl] -4-methyl-piperazine
(98) 1-Methyl-4-[5-phenyl-1-(4-thiophen-3-yl-phenyl)-1 H- 3,1 OE-08 pyrazol-4-ylmethyl]-piperazin(98) 1-Methyl-4- [5-phenyl-1- (4-thiophene-3-yl-phenyl) -1 H-3.1 OE-08 pyrazol-4-ylmethyl] piperazine
(99) 1 -[1 -(2'-Fluoro-biphenyl-4-yl)-5-(4-f luoro-phenyl)-1 H- 2,1 OE-07 pyrazol-4-ylmethyl]-4-methyl-piρerazin(99) 1 - [1 - (2'-Fluoro-biphenyl-4-yl) -5- (4-f luoro-phenyl) -1 H- 2.1 OE-07 pyrazol-4-ylmethyl] -4- methyl-piρerazin
(100) 1-[1-(4*-Fluoro-biphenyl-4-yl)-5-(4-fluoro-phenyl)-1H- 2.50E-08 pyrazol-4-ylmethyl]-4-methyl-piperazin (101) 1-[1-(2*,5'-Difluoro-biphenyl-4-yl)-5-(4-fluoro-phenyl)- 2.40E-07(100) 1- [1- (4 * -fluorobiphenyl-4-yl) -5- (4-fluoro-phenyl) -1H- 2.50E-08 pyrazol-4-ylmethyl] -4-methyl-piperazine ( 101) 1- [1- (2 *, 5'-difluorobiphenyl-4-yl) -5- (4-fluoro-phenyl) - 2.40E-07
1H-pyrazol-4-ylmethyl]-4-methyl-piperazin (102) 1 -[5-(4-Fluoro-phenyl)-1 -(4-thiophen-3-yl-phenyl)-1 H- 1 ,10E-06 pyrazol-4-ylmethyl]-4-methyl-piperazin1H-pyrazol-4-ylmethyl] -4-methyl-piperazine (102) 1 - [5- (4-Fluoro-phenyl) -1 - (4-thiophene-3-yl-phenyl) -1 H-1, 10E-06 pyrazol-4-ylmethyl] -4-methyl-piperazine
(103) 1-[1-(2'-Fluoro-biphenyl-4-yl)-5-furan-2-yl-1H-pyra∑ol-4- 2,50E-08 ylmethyl]-4-methyl-piperazin(103) 1- [1- (2'-Fluoro-biphenyl-4-yl) -5-furan-2-yl-1H-pyra∑ol-4- 2,50E-08 ylmethyl] -4-methyl-piperazine
104) 1-[1-(2'-Fluoro-biphenyl-4-yl)-5-(2-methoxy-phenyl)-1 H- 5,20E-08 pyrazol-4-ylmethyl]-4-methyl-piperazin104) 1- [1- (2'-Fluoro-biphenyl-4-yl) -5- (2-methoxyphenyl) -1 H- 5.20E-08 pyrazol-4-ylmethyl] -4-methyl-piperazine
105) 1-[5-(2-Methoxy-phenyl)-1-(4-thiophen-3-yl-phenyl)-1H- 4.60E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin105) 1- [5- (2-Methoxyphenyl) -1- (4-thiophene-3-ylphenyl) -1H- 4.60E-07 pyrazol-4-ylmethyl] -4-methyl-piperazine
106) 1-[5-(2-Fluoro-phenyl)-1-(4-pyrrol-1-yl-phenyl)-1H- 1.70E-08 pyrazol-4-ylmethyl]-4-methyl-piperazin106) 1- [5- (2-Fluoro-phenyl) -1- (4-pyrrol-1-yl-phenyl) -1H-1.70E-08 pyrazol-4-ylmethyl] -4-methyl-piperazine
107) (1-Aza-bicyclo[2.2.2]oct-3-yl)-[1-biphenyl-4-yl-5-(2- 1 ,40E-07 fluoro-phenyl)-1H-pyrazol-4-ylmethyl]-amin107) (1-Azabicyclo [2.2.2] oct-3-yl) - [1-biphenyl-4-yl-5- (2- 1, 40E-07 fluorophenyl) -1H-pyrazole-4- ylmethyl] -amine
108) 4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4,30E-08 ylmethylj-thiomorpholin 1 ,1-dioxide108) 4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4.30E-08 ylmethylj-thiomorpholine 1, 1-dioxide
109) 2-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 9.40E-08 ylmethyl]-5-methyl-2,5-diaza-bicyclo[2.2.1]heptan109) 2- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 9.40E-08 ylmethyl] -5-methyl-2,5-diaza-bicyclo [2.2 heptane .1]
110) 4-{[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,70E-07 ylmethyl]-methyl-amino}-piperidin-1-carboxylsäure ethyl ester110) 4 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 70E-07 ylmethyl] methylamino} piperidine-1-carboxylic acid ethyl ester
111) 2-{4-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 3.60E-07 ylmethyl]-piperazin-1 -ylj-acetamid111) 2- {4- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 3.60E-07 ylmethyl] piperazin-1-yl-acetamide
112) 3-{[1 -Biphen l-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2,10E-07 ylmethyl]-amino}-propionsäure methyl ester112) 3 - {[1 -Biphen l-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-2,10E-07 ylmethyl] amino} propionic acid methyl ester
113) 1-(1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4- 2.90E-07 ylmethyl)-4-methyl-piperazin113) 1- (1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4- 2.90E-07 ylmethyl) -4-methyl-piperazine
114) 1-[5-(2-Fluoro-phenyl)-1-(4-isopropyl-phenyl)-1 H- 1.20E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin114) 1- [5- (2-Fluoro-phenyl) -1- (4-isopropylphenyl) -1 H-1.20E-07 pyrazol-4-ylmethyl] -4-methyl-piperazine
115) 1 -[5-(2-Fluoro-phenyl)-1 -(4-trifluoromethoxy-phenyl)- 2.70E-07 1 H-pyrazol-4-ylmethyl]-4-methyl-piperazin115) 1 - [5- (2-Fluoro-phenyl) -1 - (4-trifluoromethoxy-phenyl) - 2.70E-07 1 H-pyrazol-4-ylmethyl] -4-methyl-piperazine
116) 1 -{5-(2-Fluoro-phenyl)-1 -|6-(4-fluoro-phenyl)-pyridin-3- 1 ,20E-07 yl]-1H-pyrazol-4-ylmethyl}-4-methyl-piperazin 117) [(1 -Biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4-ylmethyl)- 9.40E-07 aminoj-essisäure ethyl ester116) 1 - {5- (2-Fluoro-phenyl) -1 - | 6- (4-fluoro-phenyl) pyridin-3- 1, 20E-07 yl] -1H-pyrazol-4-ylmethyl} -4 -methyl-piperazine 117) [(1-Biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4-ylmethyl) - 9.40E-07 aminoj-acetic acid ethyl ester
118) 2-{[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 7,30E-07 ylmethyl]-amino}-acetamid118) 2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 7.30E-07 ylmethyl] amino} acetamide
119) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yl3- 3,00E-07 1 H-pyra∑ol-4-yl}-methanol119) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-yl3-3.00E-07 1 H-pyra∑ol-4-yl} methanol
120) 1-[5-(2-Fluoro-phenyl)-1-(4-pyridin-3-yl-phenyl)-1H- 1.70E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin120) 1- [5- (2-Fluoro-phenyl) -1- (4-pyridin-3-yl-phenyl) -1H- 1.70E-07 pyrazol-4-ylmethyl] -4-methyl-piperazine
121) 1-[5-(2-Fiuoro-phenyl)-1-(4-pyridin-4-yl-phenyl)-1 H- 7.70E-08 pyrazol-4-ylmethylJ-4-methyl-piperazin121) 1- [5- (2-Fiuoro-phenyl) -1- (4-pyridin-4-yl-phenyl) -1 H- 7.70E-08 pyrazol-4-ylmethylJ-4-methyl-piperazine
122) [1-(2',5'-Difluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl)-1H- 3.70E-07 pyrazol-4-ylmethyl]-(tetrahydro-furan-2-ylmethyl)-amin122) [1- (2 ', 5'-Difluorobiphenyl-4-yl) -5- (2-fluoro-phenyl) -1H- 3.70E-07 pyrazol-4-ylmethyl] - (tetrahydro-furan-2 ylmethyl) amine
123) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 8.30E-07 ylmethyl]-4-methansulfonyl-piperazin123) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 8.30E-07 ylmethyl] -4-methanesulfonyl-piperazine
124) {[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 2.80E-07 ylmethyl]-amino}-acetonitrile124) {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 2.80E-07 ylmethyl] amino} acetonitrile
125) 2-{4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 5.10E-07 ylmethyl]-piperazin-1-yl}-1-pyrrolidin-1-yl-ethanon125) 2- {4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 5.10E-07 ylmethyl] piperazin-1-yl} -1-pyrrolidine -1-yl-ethanone
126) 4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 7.90E-07 ylmethyl]-piperazin-1-carboxylsäure phenylamid126) 4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 7.90E-07 ylmethyl] piperazine-1-carboxylic acid phenylamide
127) N-[5-(2-Fluoro-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- 4.40E-07 pyrazol-4-ylmethyl]-N,N',N'-trimethyl-ethan-1,2-diamin127) N- [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H- 4.40E-07 pyrazol-4-ylmethyl] -N, N ', N' -trimethyl-ethane-1,2-diamine
128) 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.00E-07 ylmethyl3-amino}-N,N-dimethyl-acetamid128) 2 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-2.00E-07 ylmethyl3-amino} -N, N-dimethyl-acetamide
129) 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1.00E-07 ylmethyl]-amino}-N-(4-nitro-phenyl)-acetamid129) 2 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1.00E-07 ylmethyl] -amino} -N- (4-nitro-phenyl) - acetamide
130) 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 6.00E-07 ylmethyl3-amino}-N-methyl-acetamid130) 2 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 6.00E-07 ylmethyl3-amino} -N-methyl-acetamide
131) 4-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.00E-06 ylmethyl3-amino}-isoxazolidin-3-on131) 4 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.00E-06 ylmethyl3-amino} -isoxazolidin-3-one
132) 2-{[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 9.20E-07 ylmethyl]-methyl-amino}-acetamid (133) (1H-Benzoimidazol-2-ylmethyl)-[1-biphenyl-4-yl-5-(2- 7.60E-08 fluoro-phenyl)-1H-pyrazol-4-ylmethyl]-amin132) 2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 9.20E-07 ylmethyl] methylamino} acetamide (133) (1H-Benzoimidazol-2-ylmethyl) - [1-biphenyl-4-yl-5- (2- 7.60E-08 fluorophenyl) -1H-pyrazol-4-ylmethyl] amine
(134) [5-(2-Fluoro-phenyl)-1-(6-phenyl-pyridin-3-yl)-1H- 3,00E-07 pyrazol-4-ylmethyl]-(2-methoxy-ethyl)-methyl-amin(134) [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1H- 3.00E-07 pyrazol-4-ylmethyl] - (2-methoxy-ethyl) - methyl-amine
135) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 3,80E-07 yImethyl]-4-thiophen-3-ylmethyl-piperazin135) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 3.80E-07 yImethyl] -4-thiophene-3-ylmethyl-piperazine
136) 2-{[1 -Biphenyl-4-yl-5-(2-fluoro-ρhenyl)-1 H-pyrazol-4- 1 ,30E-07 ylmethyl]-amino}-2-cyano-acetamid136) 2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-ρhenyl) -1 H-pyrazol-4- 1, 30E-07 ylmethyl] amino} -2-cyano-acetamide
137) 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 3.70E-07 ylmethyl]-amino}-3-(3H-imidazol-4-yl)-propan-1-oI137) 2 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 3.70E-07 ylmethyl] -amino} -3- (3H-imidazole-4- yl) propan-1-oI
138) [1 -Biphenyl-4-yl-5-(2-f luoro-phenyl)-1 H-pyrazol-4- 2.40E-07 ylmethylj-isoxazol-3-yl-amin138) [1-Biphenyl-4-yl-5- (2-f luoro-phenyl) -1 H-pyrazol-4- 2.40E-07 ylmethylj-isoxazol-3-yl-amine
139) 2-{4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 2,30E-07 ylmethyl]-piperazin-1-yl}-N-ethyl-acetamid139) 2- {4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 2.30E-07 ylmethyl] piperazin-1-yl} -N-ethyl -acetamide
140) [1 -(2',5'-Difluoro-biphenyl-4-yl)-5-(2-fluoro-phenyl)-1 H- 1 ,80E-07 pyrazol-4-ylmethyl]-(1 H-pyrazoI-3-yl)-amin140) [1 - (2 ', 5'-Difluorobiphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- 1, 80E-07 pyrazol-4-ylmethyl] - (1 H- pyrazol-3-yl) -amine
141) N-{5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3- 1 ,40E-07 y!3-1 H-pyrazol-4-ylmethyl}-N,N',N'-trimethyl-ethan-1 ,2- diamin141) N- {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridine-3- 1,40E-07 y! 3-1 H-pyrazol-4-ylmethyl} -N, N ', N'-trimethyl-ethane-1,2-diamine
142) 2-(4-Fluoro-phenyl)-5-[5-(2-fluoro-phenyl)-4-pyrrolidin- 7,50E-08 1-ylmethyl-pyrazol-1-yl]-pyridin142) 2- (4-Fluoro-phenyl) -5- [5- (2-fluoro-phenyl) -4-pyrrolidine 7.50E-08 1-ylmethylpyrazol-1-yl] pyridine
143) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-ylj- 2.50E-07 1H-pyrazol-4-ylmethyl}-methyl-(1-methyl-piperidin-4- yl)-amin143) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-ylj- 2.50E-07 1H-pyrazol-4-ylmethyl} methyl- (1- methyl-piperidin-4-yl) amine
144) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yl3- 8.90E-07 1 H-pyrazol-4-ylmethyl}-pyridin-3-yl-amin144) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-yl3- 8.90E-07 1 H-pyrazol-4-ylmethyl} pyridine-3- yl-amine
145) 1-{5-(2-FIuoro-phenyl)-1-[6-(2-fluoro-phenyl)-pyridin-3- 2,20E-07 ylj-1H-pyrazol~4-ylmethyl}-pyrro!idin-2-carboxylsäure amid145) 1- {5- (2-fluorophenyl) -1- [6- (2-fluoro-phenyl) pyridine-3-2.20E-07 ylj-1H-pyrazole ~ 4-ylmethyl} pyrro! idin-2-carboxylic acid amide
146) 4-{5-(2-Fluoro-phenyl)-1-[6-(2-fluoro-phenyl)-pyridin-3- 6.00E-07 y -1H-pyrazol-4-ylmethyl}-morpholin146) 4- {5- (2-Fluoro-phenyl) -1- [6- (2-fluoro-phenyl) pyridine-3- 6.00E-07 y -1H-pyrazol-4-ylmethyl} morpholine
147) 1-[1-[6-(2,5-Difluoro-phenyl)-pyridin-3-yl]-5-(2-fluoro- 4,30E-07 phenyl)-1 H-pyrazol-4-ylmethylJ-4-methyl-piperazin147) 1- [1- [6- (2,5-Difluorophenyl) pyridin-3-yl] -5- (2-fluoro- 4.30E-07 phenyl) -1 H-pyrazol-4-ylmethylJ-4-methyl-piperazine
148) ({5-(2-Fluoro-phenyl)-1-[6-(2-fluoro-phenyl)-pyridin-3- 1 ,60E-06 ylj-1 H-pyrazol-4-ylmethyl}-amino)-essigsäure ethyl cöl"l148) ({5- (2-Fluoro-phenyl) -1- [6- (2-fluoro-phenyl) -pyridin-3- 1, 60E-06 ylj-1 H-pyrazol-4-ylmethyl} amino) -acetic acid ethyl cöl "l
149) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyra∑bl-4-yl]- 6.20E-07 4-(4-methyl-piperazin-1 -yl)-butan-1 ,3-diol149) 1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyra∑bl-4-yl] - 6.20E-07 4- (4-methyl-piperazin-1 - yl) -butane-1,3-diol
150) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyra∑ol-4-ylj- 1.30E-06 but-3-en-1-ol150) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyra∑ol-4-ylj-1.30E-06 but-3-en-1-ol
0 151) 1-(3-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 6,40E-08 ylmethylJ-amino}-propyl)-pyrrolidin-2-on0 151) 1- (3 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 6.40E-08 ylmethylJ-amino} propyl) pyrrolidin-2 -one
152) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,30E-07 ylmethylJ-(3-imidazol-1-yl-propyl)-amin152) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 30E-07 ylmethylJ- (3-imidazol-1-yl-propyl) amine
153) (2-{[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazoI-4- 1 ,10E-06 5 ylmethyl]-amino}-ethanoylamino)-essigsäure ethyl ester153) (2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazoI-4- 1, 10E-06 5 ylmethyl] amino} ethanoylamino) acetic acid ethyl ester
154) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1.70E-07 ylmethyl]-[2-(1H-imidazol-4-yl)-ethyl]-amin154) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1.70E-07 ylmethyl] - [2- (1H-imidazol-4-yl) ethyl] amine
0 155) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1.70E-06 ylmethyl]-pyrrolidin-2-carboxylsäure amid0 155) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1.70E-06 ylmethyl] pyrrolidine-2-carboxylic acid amide
156) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yt}- 3.00E-07 1 H-pyrazol-4-ylmethyl}-(2-methoxy-ethyl)-methyl-amin156) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-yt} - 3.00E-07 1 H-pyrazol-4-ylmethyl} - (2- methoxy-ethyl) -methyl-amine
157) {5-(2-Fluoro-phenyl)-1-[6-(2-fluoro-phenyl)-pyridin-3-yl]- 2.00E-06 5 1 H-pyrazol-4-ylmethyl}-(2-methoxy-ethyl)-methyl-amin157) {5- (2-Fluoro-phenyl) -1- [6- (2-fluoro-phenyl) pyridin-3-yl] - 2.00E-06 5 1 H-pyrazol-4-ylmethyl} - (2nd methoxy-ethyl) -methyl-amine
158) [1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.30E-06 ylmethyl]-pyrazin-2-yl-amin158) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.30E-06 ylmethyl] -pyrazin-2-yl-amine
159) [1-[6-(2,5-Difluoro-phenyl)-pyridin-3-yl3-5-(2-fluoro- 1 ,40E-06 0 phenyl)-1 H-pyrazol-4-ylmethyl]-(2-methoxy-ethyl)- methyl-amin159) [1- [6- (2,5-Difluorophenyl) pyridin-3-yl3-5- (2-fluoro- 1, 40E-06 0 phenyl) -1 H-pyrazol-4-ylmethyl] - (2-methoxy-ethyl) methyl amine
160) 4-Azetidin-1 -ylmethyl-1 -biphenyl-4-yl-5-(2-f luoro- 4,70E-08 phenyl)-1 H-pyra∑ole160) 4-Azetidin-1-methyl-1-biphenyl-4-yl-5- (2-f luoro-4,70E-08 phenyl) -1 H-pyraole
161) (1 -Benzyl-pyrrolidin-3-yl)-[1 -biphenyl-4-yl-5-(2-f luoro- 3,10E-07 o phenyl)-1H-pyrazoi-4-ylmethyl3-amin (162) 4-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1.20E-07 Nlmethyl]-amino}-1 -methyl-1 H-pyrrole-2-carboxylsäure methyl ester161) (1-Benzyl-pyrrolidin-3-yl) - [1 -biphenyl-4-yl-5- (2-f luoro-3,10E-07 o phenyl) -1H-pyrazoi-4-ylmethyl3-amine (162) 4 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1.20E-07 Nlmethyl] amino} -1-methyl-1 H-pyrrole- 2-carboxylic acid methyl ester
(163) 3-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyra∑ol-4- 5,10E-07 ylmethyl]-amino}-a∑epan-2-on(163) 3 - {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyra∑ol-4- 5,10E-07 ylmethyl] -amino} -a∑epan-2- on
(164) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.70E-07 ylmethylJ-piperidin-4-carboxylsäure (2-hydroxy-ethyl)- amid(164) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.70E-07 ylmethylJ-piperidine-4-carboxylic acid (2-hydroxy-ethyl) - amide
(165) C-(1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-yl)- 2.10E-08 methylamin(165) C- (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-yl) -2.10E-08 methylamine
(166) N-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazoI-4- 1.20E-06 ylmethylene]-N'-(4,5-dihydro-1 H-imidazol-2-yl)-hydrazin(166) N- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazoI-4- 1.20E-06 ylmethylene] -N '- (4,5-dihydro-1 H- imidazol-2-yl) -hydrazine
(167) {1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 2.30E-07 ylmethyl3-pyrrolidin-3-yl}-dimethyl-amin(167) {1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 2.30E-07 ylmethyl3-pyrrolidin-3-yl} dimethylamine
(168) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 1 ,60E-08 ylmethylj-methyl-(1 -methyI-pyrrolidin-3-yl)-amin(168) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 1, 60E-08 ylmethylj-methyl- (1-methylI-pyrrolidin-3-yl) - amine
(169) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl)-(1- 3.90E-08 methyl-1 H-imidazol-2-ylmethyl)-amin(169) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) - (1- 3.90E-08 methyl-1 H -imidazol-2-ylmethyl) amine
(170) (1 -Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4-ylmethyl)- 3,1 OE-08 pyrid in-4-ylmethyl-am in(170) (1-biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) - 3.1 OE-08 pyrid in-4-ylmethyl-am in
(171) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl)-(1- . 2.60E-08 methyl-1 H-pyrrol-2-ylmethyl)-amin (172) (1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4-ylmethyl)- 2.30E-08 pyridin-2-ylmethyl-amin(171) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) - (1- . 2.60E-08 methyl-1 H-pyrrol-2-ylmethyl) amine (172) ( 1-biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) - 2.30E-08 pyridin-2-ylmethyl-amine
(173) 2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl - 4,70E-07 ethanol(173) 2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl - 4.70E-07 ethanol
(174) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yl]- 3,20E-07(174) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-yl] - 3.20E-07
1 H-pyrazol-4-ylmethyl}-isoxazol-3-yl-amin1 H-pyrazol-4-ylmethyl} isoxazol-3-yl amine
(175) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yl]- 6.30E-07 1 H-pyrazol-4-ylmethyl}-pyridin-3-yl-amin(175) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridin-3-yl] - 6.30E-07 1 H-pyrazol-4-ylmethyl} pyridine- 3-yl-amine
(176) 3-{[1 -Biphenyl-4-yl-5-(2-f luoro-phenyl)-1 H-pyrazol-4- 4.60E-07 ylmethyl3-amino}-pyrrolidin-1-carboxylsäure tert-butyl ester (177) N3-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 1.80E-07 ylmethylJ-pyridin-3,4-diamin(176) 3 - {[1 -Biphenyl-4-yl-5- (2-f luorophenyl) -1 H-pyrazol-4- 4.60E-07 ylmethyl3-amino} pyrrolidine-1-carboxylic acid tert-butyl ester (177) N 3 - [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 1.80E-07 ylmethylJ-pyridine-3,4-diamine
(178) [1-Biphenyl-4-yl-5-(2-f!uoro-phenyl)-1H-pyrazol-4- 3.70E-07 ylmethylJ-(5-methyl-thiazol-2-yl)-amin(178) [1-Biphenyl-4-yl-5- (2-f! Uoro-phenyl) -1H-pyrazol-4- 3.70E-07 ylmethylJ- (5-methylthiazol-2-yl) amine
(179) [(1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4-ylmethyl)- 1 ,00E-06 aminoj-essigsäure tert-butyl ester(179) [(1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4-ylmethyl) - 1, 00E-06 aminoj-acetic acid tert-butyl ester
(180) [(1 -Biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4-ylmethyl)- 9.20E-07 methyl-aminoj-essigsäure tert-butyl ester(180) [(1-Biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4-ylmethyl) - 9.20E-07 methyl-aminoj-acetic acid tert-butyl ester
(181) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl)-(5- 2,40E-07 methyl-isoxazol-3-ylmethyl)-amin(181) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) - (5- 2.40E-07 methyl-isoxazol-3-ylmethyl) amine
(182) 4-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 5.80E-08 ylmethyl]-piperazin-1-carboxylsäure ethyl ester(182) 4- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 5.80E-08 ylmethyl] piperazine-1-carboxylic acid ethyl ester
(183) 3-[(1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4- 8.30E-07 ylmethyl)-amino]-propionsäure methyl ester(183) 3 - [(1-Biphenyl-4-yl-5-pyridin-3-yl-1H-pyrazol-4- 8.30E-07 ylmethyl) amino] propionic acid methyl ester
(184) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 7.50E-08 ylmethyl]-4-pyridin-4-ylmethyl-piperazin (185) 4-{2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 4.00E-08 yl]-ethyl}-morpholin (186) 5-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pγrazol-4- 6.30E-07 ylmethyl3-amino}-3H-imidazole-4-carboxylsäure amid(184) 1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 7.50E-08 ylmethyl] -4-pyridin-4-ylmethyl-piperazine (185) 4- {2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 4.00E-08 yl] ethyl} morpholine (186) 5 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pγrazol-4- 6.30E-07 ylmethyl3-amino} -3H-imidazole-4-carboxylic acid amide
(187) [1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 5.90E-07 ylmethyl3-(1 ,3,5-trimethyl-1 H-pyrazol-4-yl)-amin(187) [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4- 5.90E-07 ylmethyl3- (1, 3,5-trimethyl-1 H-pyrazol-4- yl) -amine
(188) 2-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl3- 1 ,40E-06 ethylamin(188) 2- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl3-1, 40E-06 ethylamine
(189) 1-Biphenyl-4-yl-4-chloromethyl-5-(2-fluoro-phenyl)-1 H- 1 ,10E-06 pyrazole(189) 1-Biphenyl-4-yl-4-chloromethyl-5- (2-fluoro-phenyl) -1 H-1, 10E-06 pyrazole
(190) 6-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 5.20E-07 ylmethyl3-amino}-3-aza-bicyclo[3.1.0]hexan-3- carboxylsäure tert-butyl ester(190) 6 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 5.20E-07 ylmethyl3-amino} -3-aza-bicyclo [3.1.0 ] hexane-3-carboxylic acid tert-butyl ester
(191) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4- 2.00E-07 ylmethylJ-1 H-pyridin-2-on(191) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4-2.00E-07 ylmethylJ-1H-pyridin-2-one
(192) (3-Aza-bicyclo[3.1.0]hex-6-yl)-[1-biphenyl-4-yl-5-(2- 3.20E-07 fluoro-phenyI)-1H-pyrazol-4-ylmethyl3-amin(192) (3-Azabicyclo [3.1.0] hex-6-yl) - [1-biphenyl-4-yl-5- (2-3.20E-07 fluoro-phenyl) -1H-pyrazol-4-ylmethyl3-amine
193) 1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1H-pyrazol-4-yl]- 3.60E-07 1 -morpholin-4-yl-methanon193) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-pyrazol-4-yl] - 3.60E-07 1 -morpholin-4-yl-methanone
194) N5-{5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3- 5.90E-07 yl3-1 H-pyrazol-4-ylmethyl}-pyridin-2,5-diamin194) N 5 - {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridine-3- 5.90E-07 yl3-1 H-pyrazol-4-ylmethyl} pyridine -2,5-diamine
195) 3-{1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- 6.60E-08 ylmethyl3-piperidin-4-ylmethyl}-pyridin195) 3- {1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- 6.60E-08 ylmethyl3-piperidin-4-ylmethyl} pyridine
196) {5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3-yl3- 1 ,20E-06 1H-pyrazol-4-ylmethyl}-pyrazin-2-yl-amin196) {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) -pyridin-3-yl3-1, 20E-06 1H-pyrazol-4-ylmethyl} -pyrazine-2- yl-amine
197) N-{5-(2-Fluoro-phenyl)-1-[6-(4-fluoro-phenyl)-pyridin-3- 1 ,30E-06 yl3-1 H-pyrazol-4-ylmethyl}-pyrimidin-2,5-diamin197) N- {5- (2-Fluoro-phenyl) -1- [6- (4-fluoro-phenyl) pyridine-3- 1, 30E-06 yl3-1 H-pyrazol-4-ylmethyl} pyrimidine -2,5-diamine
(198) 1-Methyl-4-[1-(6-phenyl-pyridin-3-yl)-5-pyridin-3-yl-1 H- 1.40E-07 pyrazol-4-ylmethyl]-piperazin(198) 1-Methyl-4- [1- (6-phenyl-pyridin-3-yl) -5-pyridin-3-yl-1 H-1.40E-07 pyrazol-4-ylmethyl] piperazine
(199) 1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- carbonsäureethylester(199) 1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazole-4-carboxylic acid ethyl ester
(200) [1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazol-4- ylmethylene3-(4-methyl-piperazin-1-yl)-amin(200) [1-Biphenyl-4-yl-5- (2-f fluorophenyl) -1 H-pyrazol-4-ylmethylene3- (4-methyl-piperazin-1-yl) amine
(201) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-4-methyl-piperazin(201) 1- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(202) {[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-essigsäure-tert-butylester (203) 3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-thiazolidin(202) {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] amino} acetic acid tert-butyl ester (203) 3- [1-biphenyl -4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] thiazolidine
(204) 4-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-2,6-dimethyl-morpholin (205) 3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4-yl]- acrylsäure(204) 4- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] -2,6-dimethyl-morpholine (205) 3- [1-biphenyl -4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-yl] acrylic acid
(206) 3-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4-yl]- acrylsäureethylester(206) 3- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-yl] ethyl acrylate
(207) 3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4-yl3- prop-2-en-1-ol (208) 1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazoI-3- carbonsäureethylester(207) 3- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-yl3-prop-2-en-1-ol (208) 1-Biphenyl-4-yl-5- (2-fluorous phenyl) -1 H-pyrazoI-3-carboxylic acid ethyl ester
(209) [1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-3-yl]- methanol(209) [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-3-yl] methanol
(210) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-pyrrolidin-2-carbonsäure-tert-butylester(210) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] pyrrolidine-2-carboxylic acid tert-butyl ester
(211) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-propionsäure-tert-butylester(211) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} propionic acid tert-butyl ester
1 -[1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazol-4- ylmethyl]-3-(3-methoxy-phenyl)-piperidin1 - [1 -Biphenyl-4-yl-5- (2-fluorous phenyl) -1 H-pyrazol-4-ylmethyl] -3- (3-methoxyphenyl) piperidine
1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-3-cyclohexylmethyl-piperidin1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl3-3-cyclohexylmethyl-piperidine
8-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-1 ,4-dioxa-8-aza-spiro[4.5]decan8- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] -1, 4-dioxa-8-aza-spiro [4.5] decane
2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-3-methyl-buttersäure-tert-butylester2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] amino} -3-methyl-butyric acid tert-butyl ester
1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-2-methyl-piperidin1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] -2-methyl-piperidine
5-(2-Fluor-phenyl)-1 -(4-nitro-phenyl)-1 H-pyrazol-4- carbonsäureethylester5- (2-Fluoro-phenyl) -1 - (4-nitro-phenyl) -1 H-pyrazole-4-carboxylic acid ethyl ester
1 -(4-Cyano-phenyl)-5-(2-fluor-phenyl)-1 H-pyrazol-4- carbonsäureethylester1 - (4-Cyano-phenyl) -5- (2-fluoro-phenyl) -1 H-pyrazole-4-carboxylic acid ethyl ester
5-(2-Fluor-phenyl)-1-[4-(1 H-tetrazol-5-yl)-phenyl]-1 H- pyrazol-4-carbonsäureethylester5- (2-Fluoro-phenyl) -1- [4- (1 H-tetrazol-5-yl) phenyl] -1 H -pyrazole-4-carboxylic acid ethyl ester
1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-piperidin-4-on1 - [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] piperidin-4-one
{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-methyl-amino}-essigsäure- tert-butylester{[1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] methylamino} acetic acid, tert-butyl ester
5-(2-Fluor-phenyl)-1-[4-(N-hydroxycarbamimidoyl)- phenyl3-1 H-pyrazol-4-carbonsäureethylester5- (2-Fluoro-phenyl) -1- [4- (N-hydroxycarbamimidoyl) phenyl3-1 H-pyrazole-4-carboxylic acid ethyl ester
5-(2-Fluor-phenyl)-1-[4-(5-methyl-[1,2,4]oxadiazol-3- yl)-phenyl]-1 H-pyrazol-4-carbonsäureethylester (224) 1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- carbaldehyd O-mefhyl-oxime5- (2-Fluoro-phenyl) -1- [4- (5-methyl- [1,2,4] oxadiazol-3-yl) phenyl] -1 H-pyrazole-4-carboxylic acid ethyl ester (224) 1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazole-4-carbaldehyde O-methyl oxime
(225) 1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- carbaldehyd O-allyl-oxime(225) 1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazole-4-carbaldehyde O-allyl oxime
(226) 4-[5-(2-Fluor-phenyl)-1 -(S' '.δ'-trimethoxy-biphenyM- yl)-1H-pyrazol-4-y!methyl3-morpholin(226) 4- [5- (2-Fluorophenyl) -1 - (S ".δ'-trimethoxy-biphenyM-yl) -1H-pyrazol-4-y! Methyl3-morpholine
(227) 4-[5-(2-Fluor-phenyl)-1-(4'-trifluormethyl-biphenyl-4-yl)- 1 H-pyrazol-4-ylmethyl3-morpholin(227) 4- [5- (2-Fluorophenyl) -1- (4'-trifluoromethyl-biphenyl-4-yl) -1 H-pyrazol-4-ylmethyl3-morpholine
(228) 4'-[5-(2-Fluor-phenyl)-4-morpholin-4-ylmethyl-pyrazol- 1 -yl3-biphenyl-2-carbonitrile(228) 4 '- [5- (2-Fluoro-phenyl) -4-morpholin-4-ylmethyl-pyrazol-1-yl3-biphenyl-2-carbonitrile
(229) 4-[1-(2'-Chlor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-y!methyl]-morpholin(229) 4- [1- (2'-Chlorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-y! Methyl] morpholine
(230) 4-[1 -(3,,5*-Dichlor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl3-morpholin(230) 4- [1 - (3 , 5 * -Dichlorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-morpholine
(231) 4-[5-(2-Fluor-phenyl)-1-(4'-methoxy-biphenyl-4-yl)-1 H- pyrazol-4-ylmethylj-morpholin (232) 4-[1-(3',4,-Difluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl]-morpholin(231) 4- [5- (2-Fluorophenyl) -1- (4'-methoxy-biphenyl-4-yl) -1 H -pyrazol-4-ylmethylj-morpholine (232) 4- [1- ( 3 ', 4 , -Difluorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl] morpholine
(233) 4-[5-(2-Fluor-phenyl)-1-(4'-methyl-biphenyl-4-yl)-1H- pyrazol-4-ylmethyl]-morpholin(233) 4- [5- (2-fluorophenyl) -1- (4'-methyl-biphenyl-4-yl) -1H-pyrazol-4-ylmethyl] morpholine
(234) 4-[5-(2-Fluor-phenyl)-1-(3,-methoxy-biphenyl-4-yl)-1 H- pyrazol-4-ylmethylj-morpholin(234) 4- [5- (2-Fluoro-phenyl) -1- (3 , -methoxy-biphenyl-4-yl) -1 H-pyrazol-4-ylmethylj-morpholine
(235) 4-[1 -(3'-Chlor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl]-morpholin(235) 4- [1 - (3'-Chlorobiphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H -pyrazol-4-ylmethyl] morpholine
(236) 4-[5-(2-Fluor-phenyl)-1-(2'-trifluormethyl-biphenyl-4-yl)- 1 H-pyrazol-4-ylmethyl]-morpholin(236) 4- [5- (2-Fluorophenyl) -1- (2'-trifluoromethyl-biphenyl-4-yl) -1 H-pyrazol-4-ylmethyl] morpholine
(237) 4-[5-(2-Fluor-phenyl)-1 -(2'-methoxy-biphenyl-4-yl)-1 H- pyrazol-4-ylmethyl]-morpholin(237) 4- [5- (2-Fluorophenyl) -1 - (2'-methoxy-biphenyl-4-yl) -1 H-pyrazol-4-ylmethyl] morpholine
(238) 4-[1-(3'-Ethoxy-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyra∑ol-4-ylmethyl]-morpholin(238) 4- [1- (3'-Ethoxy-biphenyl-4-yl) -5- (2-fluorophenyl) -1 H-pyra∑ol-4-ylmethyl] morpholine
(239) 4-[1-(2'-Fluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl]-morpholin(239) 4- [1- (2'-fluoro-biphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- pyrazol-4-ylmethyl] -morpholine
240) 4-[1-[4-(2,3-Dihydro-benzo[1 ,43dioxin-6-yl)-phenyl3-5- (2-fluor-phenyl)-1H-pyrazol-4-ylmethyl]-morpholin240) 4- [1- [4- (2,3-Dihydro-benzo [1,43-dioxin-6-yl) phenyl3-5- (2-fluorophenyl) -1H-pyrazol-4-ylmethyl] morpholine
241) 4-[5-(2-Fluor-phenyl)-1-(4-thiophen-3-yI-phenyl)-1 H- pyrazol-4-ylmethyl]-morpholin241) 4- [5- (2-Fluorophenyl) -1- (4-thiophene-3-yI-phenyl) -1 H -pyrazol-4-ylmethyl] morpholine
242) 4-[1-(4-Butyl-phenyl)-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-morpholin242) 4- [1- (4-Butylphenyl) -5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethylj-morpholine
243) 4'-[5-(2-Fluor-phenyl)-4-morpholin-4-ylmethyl-pyrazol- 1-yl]-biphenyl-4-carbonitrile243) 4 '- [5- (2-fluorophenyl) -4-morpholin-4-ylmethylpyrazol-1-yl] biphenyl-4-carbonitrile
244) 4'-[5-(2-Fluor-phenyl)-4-morpholin-4-ylmethyl-pyrazol- 1 -yl]-biphenyl-3-carbonitrile244) 4 '- [5- (2-fluoro-phenyl) -4-morpholin-4-ylmethyl-pyrazol-1-yl] -biphenyl-3-carbonitrile
(245) 4-[1-(3',5'-Difluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1H- pyrazol-4-ylmethyl]-morpholin(245) 4- [1- (3 ', 5'-Difluorobiphenyl-4-yl) -5- (2-fluorophenyl) -1H-pyrazol-4-ylmethyl] morpholine
(246) 4-[1 -(2,,4*-Difluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethylj-morpholin(246) 4- [1 - (2, 4 * difluoro-biphenyl-4-yl) -5- (2-fluoro-phenyl) -1 H- pyrazol-4-ylmethylj-morpholine
(247) 4-[1-(2',5'-Difluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl3-morpholin(247) 4- [1- (2 ', 5'-difluorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-morpholine
(248) 4-[1-(4'-Chlor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl]-morpholin(248) 4- [1- (4'-Chlorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl] morpholine
(249) 4-[5-(2-Fluor-phenyl)-1-(3,,4',5'-trifluor-biphenyl-4-yl)- I H-pyrazol-4-ylmethylj-morpholin (250) 5-(2-Fluor-phenyl)-1-(4-trifluormethyl-phenyl)-1 H- pyrazol-4-carbonsäureethylester(249) 4- [5- (2-fluoro-phenyl) -1- (3, 4 ', 5'-trifluoro-biphenyl-4-yl) - I H-pyrazol-4-ylmethylj-morpholin (250) 5- (2-Fluoro-phenyl) -1- (4-trifluoromethyl-phenyl) -1 H-pyrazole-4-carboxylic acid ethyl ester
(251) 4-[5-(2-Fluor-phenyl)-1-p-tolyl-1H-pyrazol-4-ylmethyl]- morpholin (252) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-methyl-aminoj-essigsäure(251) 4- [5- (2-Fluoro-phenyl) -1-p-tolyl-1H-pyrazol-4-ylmethyl] - morpholine (252) {[1-biphenyl-4-yl-5- (2- fluorophenyl) -1 H-pyrazol-4-ylmethylj-methyl-aminoj-acetic acid
(253) 1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-pyrrolidin-2-carbonsäure(253) 1 - [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] pyrrolidine-2-carboxylic acid
(254) 2-{[1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-3-methyl-buttersäure (255) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyfj-aminoj-propionsäure(254) 2 - {[1 -Biphenyl-4-yl-5- (2-f fluorophenyl) -1 H -pyrazol-4-ylmethyl3-amino} -3-methylbutyric acid (255) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyfj-aminoj-propionic acid
(256) {[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-methyl-amino}-morpholin-4-yl-ethanon (257) 5-(2-Fluor-phenyl)-1-(4-imidazol-1-yl-phenyl)-1H- pyrazol-4-carbonsäureethylester(256) {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl3-methyl-amino} -morpholin-4-yl-ethanone (257) 5- ( 2-Fluoro-phenyl) -1- (4-imidazol-1-yl-phenyl) -1H-pyrazole-4-carboxylic acid ethyl ester
(258) [5-(2-Fluor-phenyl)-1 -(4-imida∑ol-1 -yl-phenyl)-1 H- pyrazol-4-yl]-methanol (259) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-pyrrolidin-2-carbonsäureamid(258) [5- (2-fluorophenyl) -1 - (4-imidol-1-yl-phenyl) -1 H-pyrazol-4-yl] -methanol (259) 1- [1-biphenyl -4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] pyrrolidine-2-carboxamide
(260) [5-(2-Fluor-phenyl)-1-(4-trifluormethyl-phenyl)-1 H- pyrazol-4-yl]-methanol(260) [5- (2-Fluorophenyl) -1- (4-trifluoromethylphenyl) -1 H -pyrazol-4-yl] methanol
(261) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-essigsäureethylester(261) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} ethyl acetate
(262) (2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-ethyl)-carbamidsäure-tert-butylester(262) (2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-amino} -ethyl) carbamic acid tert-butyl ester
(263) 4-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-piperidin-1 -carbonsäure-tert- butylester(263) 4 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl3-amino} -piperidine-1-carboxylic acid tert-butyl ester
(264) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylJ-piperidin-4-carbonsäureethylester(264) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethylJ-piperidine-4-carboxylic acid ethyl ester
(265) 4-[5-(2-Fluor-phenyl)-1 -(4-imidazol-1 -yl-phenyl)-1 H- pyrazol-4-ylmethylj-morpholin(265) 4- [5- (2-Fluoro-phenyl) -1 - (4-imidazol-1-yl-phenyl) -1 H-pyrazol-4-ylmethylj-morpholine
(266) 1-[5-(2-Fluor-phenyl)-1-(4-imidazol-1-yl-phenyl)-1H- pyrazol-4-ylmethyli-4-methyl-piperazin(266) 1- [5- (2-Fluoro-phenyl) -1- (4-imidazol-1-yl-phenyl) -1H-pyrazol-4-ylmethyli-4-methyl-piperazine
(267) {[5-(2-Fluor-phenyl)-1 -(4-imidazol-1 -yl-phenyl)-1 H- pyrazol-4-ylmethyl]-amino}-essigsäureethylester(267) {[5- (2-Fluoro-phenyl) -1 - (4-imidazol-1-yl-phenyl) -1 H-pyrazol-4-ylmethyl] amino} ethyl acetate
(268) 1 -[1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazol-4- ylmethyl]-piperidin-4-carbonsäure(268) 1 - [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] piperidine-4-carboxylic acid
(269) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-essigsäure(269) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-amino} acetic acid
(270) 5-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-2,5-diaza-bicyclo[2.2.1]heptan-2- carbonsäure tert-butylester(270) 5- [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4- ylmethyl] -2,5-diaza-bicyclo [2.2.1] heptane-2-carboxylic acid tert-butyl ester
271 ) 4-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-piperazin-l-cärbaldehyd271) 4- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethylj-piperazin-l-carbaldehyde
272) {1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyra∑ol-4- ylmethyl3-3-oxo-piperazin-2-yl}-essigsäureethy!ester272) {1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyra∑ol-4-ylmethyl3-3-oxopiperazin-2-yl} ethyl acetate
273) 4-[1 -Biphenyl-4-yl-5-(2-fluor-phenyI)-1 H-pyrazol-4- ylmethylj-thiomorpholin273) 4- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyI) -1 H-pyrazol-4-ylmethylj-thiomorpholine
274) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylJ-pyridin-S-yl-amin274) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethylJ-pyridin-S-yl-amine
275) 1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-imidazolidin-2-on275) 1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] imidazolidin-2-one
(276) 4-[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-thiomorpholin 1-oxide(276) 4- [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethylj-thiomorpholine 1-oxide
(277) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-succinsäure dimethylester(277) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} succinic acid dimethyl ester
(278) 4-[1 -(2*,6'-Difluor-biphenyl-4-yl)-5-(2-fluor-phenyl)-1 H- pyrazol-4-ylmethyl3-morpholin(278) 4- [1 - (2 * , 6'-difluorobiphenyl-4-yl) -5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-morpholine
(279) 2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-malonamid(279) 2 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} malonamide
(280) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H-pyrazol-4- ylmethylj-carbamoylmethyl-carbamidsäureethylester (281) 4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H-pyrazol-4- ylmethyl]-morpholin-3,5-dion(280) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H-pyrazol-4-ylmethylj-carbamoylmethyl-carbamic acid ethyl ester (281) 4- [1-biphenyl-4-yl-5- ( 2-fluorophenyl) -1H-pyrazol-4-ylmethyl] morpholine-3,5-dione
(282) 1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-piperidin-4-on O-methyl-oxime (283) 4-[5-(2-Fluor-phenyl)-1-(4-isopropyl-phenyl)-1 H- pyrazol-4-ylmethylj-morpholin(282) 1 - [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethylj-piperidin-4-one O-methyl-oxime (283) 4- [5 - (2-Fluorophenyl) -1- (4-isopropylphenyl) -1 H -pyrazol-4-ylmethylj-morpholine
(284) {[5-(2-Fluor-phenyl)-1-(4-isopropyl-phenyl)-1 H-pyrazol- 4-ylmethyl]-amino}-essigsäureethylester(284) {[5- (2-Fluorophenyl) -1- (4-isopropylphenyl) -1 H-pyrazol-4-ylmethyl] amino} ethyl acetate
(285) 4-[5-(2-Fluor-phenyl)-1-(4-trifluormethoxy-phenyl)-1 H- pyra∑ol-4-ylmethyl3-morpholin 286) {[5-(2-Fluor-phenyl)-1 -(4-trif luormethoxy-phenyl)-1 H- pyrazol-4-ylmethyl]-amino}-essigsäureethylester(285) 4- [5- (2-Fluorophenyl) -1- (4-trifluoromethoxyphenyl) -1 H-pyra∑ol-4-ylmethyl3-morpholine 286) {[5- (2-Fluorophenyl) -1 - (4-trifluoromethoxyphenyl) -1 H -pyrazol-4-ylmethyl] amino} ethyl acetate
287) 5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-carbonsäureethylester287) 5- (2-fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazole-4-carboxylic acid ethyl ester
288) [5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-yl]-methanol288) [5- (2-Fluoro-phenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H-pyrazol-4-yl] methanol
289) 4-[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethylj-morpholin289) 4- [5- (2-fluorophenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H-pyrazol-4-ylmethylj-morpholine
290) {[5-(2-Fiuor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-amino}-essigsäure tert-butylester290) {[5- (2-Fiorophenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] amino} acetic acid tert-butyl ester
291 ) {[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-y!)-1 H- pyrazol-4-ylmethyl]-amino}-essigsäure291) {[5- (2-Fluoro-phenyl) -1 - (6-phenyl-pyridin-3-y!) - 1 H -pyrazol-4-ylmethyl] amino} acetic acid
(292) 1-[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H-(292) 1- [5- (2-fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H-
15 pyrazol-4-ylmethyl]-piperazin15 pyrazol-4-ylmethyl] piperazine
(293) 1-[5-(2-FIuor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-4-methyl-piperazin(293) 1- [5- (2-fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] -4-methyl-piperazine
(294) 4-[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- 20 pyrazol-4-ylmethyt]-piperazin-1 -carbonsäure tert- butylester(294) 4- [5- (2-Fluoro-phenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H-20 pyrazol-4-ylmethyt] piperazin-1-carboxylic acid tert-butyl ester
(295) 1-[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-piperidin-4-carbonsäureethylester(295) 1- [5- (2-Fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] piperidine-4-carboxylic acid ethyl ester
(296) 2-{4-[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- 25 pyrazol-4-ylmethyl]-piperazin-1 -yl}-nicotinonitrile(296) 2- {4- [5- (2-fluoro-phenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H- 25 pyrazol-4-ylmethyl] piperazin-1-yl} -nicotinonitrile
(297) (2-{[5-(2-Fluor-phehyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl3-amino}-ethyl)-carbamidsäuretert- butylester(297) (2 - {[5- (2-Fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl3-amino} -ethyl) -carbamic acid tert-butyl ester
30 (298) 4-{[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-amino}-piperidin-1-carbonsäure tert-butylester30 (298) 4 - {[5- (2-fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] amino} piperidine-1-carboxylic acid tert-butyl ester
(299) 5-{[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyi]-amino}-furan-2- carbonsäuremethylester(299) 5 - {[5- (2-Fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyi] amino} furan-2-carboxylic acid methyl ester
ΌΌΌΌ
(300) 4-{[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-amino}-piperidin-1- carbonsäureethylester(300) 4 - {[5- (2-fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H- pyrazol-4-ylmethyl] amino} piperidine-1-carboxylic acid ethyl ester
301) N1-[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1H- pyra∑ol-4-ylmethyl]-ethan-1,2-diarnin301) N1- [5- (2-fluorophenyl) -1- (6-phenyl-pyridin-3-yl) -1H-pyra∑ol-4-ylmethyl] ethane-1,2-diarnine
302) [5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyra∑ol-4-ylmethyl]-piperidin-4-yl-amin302) [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H-pyra∑ol-4-ylmethyl] piperidin-4-yl-amine
303) 1 -[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- pyra∑ol-4-ylmethyl3-piperidin-4-carbonsäure303) 1 - [5- (2-fluoro-phenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H-pyra∑ol-4-ylmethyl3-piperidine-4-carboxylic acid
304) 4-Ethyl-1 -[5-(2-fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)- 1H-pyrazol-4-ylmethyl]-piperidin-4-ol304) 4-Ethyl-1 - [5- (2-fluoro-phenyl) -1 - (6-phenyl-pyridin-3-yl) - 1H-pyrazol-4-ylmethyl] piperidin-4-ol
305) 5-[5-(2-Fluor-phenyl)-1 -(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl}-2-oxa-5-aza-bicyclo[2.2.1 ]heptan305) 5- [5- (2-Fluorophenyl) -1 - (6-phenyl-pyridin-3-yl) -1 H-pyrazol-4-ylmethyl} -2-oxa-5-aza-bicyclo [2.2 .1] heptane
(306) {4-[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-piperazin-1-yl}- essigsäureethylester(306) {4- [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H-pyrazol-4-ylmethyl] piperazin-1-yl} ethyl acetate
(307) {4-[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-piperazin-1-yl}-essigsäure (308) 5-[5-(2-Fluor-phenyl)-4-piperidin-1 -ylmethyl-pyrazoI-1 ■ yl]-2-phenyl-pyridin(307) {4- [5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H-pyrazol-4-ylmethyl] piperazin-1-yl} acetic acid ( 308) 5- [5- (2-fluoro-phenyl) -4-piperidin-1-ylmethyl-pyrazol-1 ■ yl] -2-phenyl-pyridine
(309) 4-{5-(2-Fluor-phenyl)-1 -[6-(4-fluor-phenyl)-pyridin-3- yl]-1 H-pyrazol-4-yImethyl}-morpholin(309) 4- {5- (2-Fluorophenyl) -1 - [6- (4-fluorophenyl) pyridin-3-yl] -1 H-pyrazol-4-yImethyl} morpholine
(310) ({5-(2-Fluor-phenyl)-1-[6-(4-fluor-phenyl)-pyridin-3-yl3- 1 H-pyrazol-4-ylmethyl}-amino)-essigsäureethylester(310) ({5- (2-Fluorophenyl) -1- [6- (4-fluorophenyl) pyridin-3-yl3-1 H-pyrazol-4-ylmethyl} amino) ethyl acetate
(311) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-essigsäure(311) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} acetic acid
(312) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylj-aminoj-essigsäure-tert-butylester(312) {[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H -pyrazol-4-ylmethylj-aminoj-acetic acid tert-butyl ester
(313) {[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- pyrazol-4-ylmethyl]-amino}-essigsäure-tert-butylester(313) {[5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] amino} acetic acid tert-butyl ester
(314) {[5-(2-Fluor-phenyl)-1-(6-phenyl-pyridin-3-yl)-1 H- py razol-4-y lmethyl]-am i no}-essigsä u re(314) {[5- (2-Fluoro-phenyl) -1- (6-phenyl-pyridin-3-yl) -1 H -pyrazol-4-ylmethyl] -am i no} acetic acid
(315) [(1 -Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4-ylmethyl)- amino]-essigsäure-tert-butylester(315) [(1-biphenyl-4-yl-5-phenyl-1 H-pyrazol-4-ylmethyl) - amino] -acetic acid tert-butyl ester
(316) {[Biphenyl-4-yl-(bis trifluormethyl-phenyI)-1 H-pyrazol-4- ylmethylJ-amino}-essigsäure-tert-butylester(316) {[Biphenyl-4-yl- (bis trifluoromethylphenyI) -1 H -pyrazol-4-ylmethylJ-amino} acetic acid tert-butyl ester
(317) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethylJ-pyrrolidin-2-carbonsäure-tert-butylester(317) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethylJ-pyrrolidine-2-carboxylic acid tert-butyl ester
(318) 2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-propionsäure-tert-butylester(318) 2 - {[1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} propionic acid tert-butyl ester
(319) 2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-3-methyl-butyric acid-tert-butylester(319) 2 - {[1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} -3-methyl-butyric acid tert-butyl ester
(320) {[Biphenyl-4-yl-(bis-trifluormethyl-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-essigsäure(320) {[Biphenyl-4-yl- (bis-trifluoromethylphenyl) -1 H -pyrazol-4-ylmethyl3-amino} acetic acid
(321) [(1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4-ylmethyl)- aminoj-essigsäure(321) [(1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-ylmethyl) aminoj-acetic acid
(322) {[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-methyl-amino}-essigsäure-tert-butylester(322) {[1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl3-methylamino} acetic acid tert-butyl ester
(323) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-methyl-amino}-essigsäure(323) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl3-methylamino} acetic acid
(324) 1 -[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-pyrrolidin-2-carbonsäure(324) 1 - [1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl] pyrrolidine-2-carboxylic acid
(325) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-3-methyl-butansäure(325) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} -3-methylbutanoic acid
(326) 2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-propionsäure(326) 2 - {[1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] amino} propionic acid
(327) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-methyl-amino}-morpholin-4-yl-ethanon (328) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-pyrrolidin-2-carbonsäureamid(327) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazol-4-ylmethyl] methylamino} morpholin-4-ylethanone (328) 1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] pyrrolidine-2-carboxamide
(329) {[1 -Biphenyi-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl3-amino}-essigsäureethylester(329) {[1 -Biphenyi-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl3-amino} acetic acid ethyl ester
(330) {[5-(2-FIuor-phenyl)-1 -(4-imidazol-1 -yl-phenyl)-1 H- pyrazol-4-ylmethyl3-amino}-essigsäureethylester 331 ) {[1 -Biphenyl-4-yl-5-(2-f luor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-essigsäure(330) {[5- (2-fluorophenyl) -1 - (4-imidazol-1-yl-phenyl) -1 H -pyrazol-4-ylmethyl3-amino} -acetate 331) {[1 -Biphenyl-4-yl-5- (2-f fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} acetic acid
332) {1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyra∑ol-4- ylmethyl3-3-oxo-piperazin-2-yl}-essigsäureethylester332) {1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyra∑ol-4-ylmethyl3-3-oxopiperazin-2-yl} acetic acid ethyl ester
333) 2-{[1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazoI-4- ylmethyl]-amino}-succinsäuredimethyl ester333) 2 - {[1 -Biphenyl-4-yl-5- (2-fluorophenyl) -1 H -pyrazoI-4-ylmethyl] amino} succinic acid dimethyl ester
334) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-amino}-malonamid334) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] amino} malonamide
335) [1 -Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-carbamoylmethyl-carbamidsäureethylester335) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] carbamoylmethyl carbamic acid ethyl ester
336) {[5-(2-F!uor-phenyl)-1 -(4-isopropyl-phenyl)-1 H-pyrazol- 4-ylmethyl]-amino}-essigsäureethylester336) {[5- (2-F! Uorophenyl) -1 - (4-isopropylphenyl) -1 H -pyrazol-4-ylmethyl] amino} acetic acid ethyl ester
(337) {[5-(2-Fluor-phenyl)-1-(4-trifluormethoxy-phenyl)-1 H- pyrazol-4-ylmethyl3-amino}-essigsäureethylester(337) {[5- (2-Fluorophenyl) -1- (4-trifluoromethoxyphenyl) -1 H -pyrazol-4-ylmethyl3-amino} acetic acid ethyl ester
(338) ({5-(2-Fluor-phenyl)-1-[6-(4-fluor-phenyl)-pyridin-3-yl]- 1H-pyrazol-4-ylmethyl}-amino)-essigsäureethylester(338) ({5- (2-Fluorophenyl) -1- [6- (4-fluorophenyl) pyridin-3-yl] -1H-pyrazol-4-ylmethyl} amino) ethyl acetate
(339) 4-(1 -Biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4- ylmethyl)-morpholin(339) 4- (1-biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4-ylmethyl) morpholine
R1 R2 XR 1 R 2 X
(340) CH(340) CH
XJ \^~" XJ \ ^ ~ "
(341) CH(341) CH
F~ " \_ ~ F ~ " \ _ ~
(342) CH(342) CH
Q~~ X Q ~~ X
(344) w II \ CH //(344) w II \ CH //
(3»j4-r9»)(3 »j4-r9»)
(350)(350)
(356) /=\ /=\ CH(356) / = \ / = \ CH
F ü" For "
(358) CH(358) CH
Nc- " Q~ Nc - " Q ~
(362) CF3 CH(362) CF 3 CH
(363) """O- CF3 CH(363) """O-CF 3 CH
(365) N x)~ \_(365) N x) ~ \ _
(366) . N(366). N
F→ ~ \_ F → ~ \ _
(369) -N\_ N II /> — \_(369) - N \ _ N II /> - \ _
(381) N(381) N
F^C}~ x F ^ C} ~ x
(382) N(382) N
Q~ XXQ ~ XX
(385) J^~ X) N(385) J ^ ~ X) N
(386) N(386) N
F→Q- X F → Q-X
(387) CF3 N ~ (387) CF 3 N ~
(388) CF3 N °- ~ (388) CF 3 N ° - ~
(389) r CF3 N(389) r CF 3 N
Beispiele 390 - 439: Examples 390 - 439:
R1 R2 XR 1 R 2 X
(390) ~cτ-r w //(390) ~ cτ-rw //
(407) CH(407) CH
C^~ Ch C ^ ~ Ch
(409) CH ιι > — X(409) CH ιι> - X
(410) _y X) CH(410) _y X) CH
(411)(411)
F j~ X) CH F j ~ X) CH
(412) CF3 CH(412) CF 3 CH
C^C ^
(413) m^ ~ CF3 CH(413) m ^ ~ CF 3 CH
(414) ϋr CF3 CH(414) CFr CF 3 CH
(416) > x N(416)> x N
X-JX-J
(431) =\ =\ N(431) = \ = \ N
(432) N(432) N
N— J ^— (433) _y==v_ rv_ N (434) -N\ ^x N N— J ^ - (433) _y == v_ rv_ N (434) - N \ ^ x N
(436) (436)
F~O~ X) N F ~ O ~ X) N
(437) CF3 N(437) CF 3 N
Q~ Q ~
(438) CF3 N(438) CF 3 N
NC~ ~NC ~ ~
Beispiele 440 - 489:Examples 440-489:
R1 R2 XR 1 R 2 X
(440) CH _y \_(440) CH _y \ _
(441) CH(441) CH
F~ ~ _ F ~ ~ _
(442) CH(442) CH
O- _O- _
(444) CH(444) CH
N "~ _yN "~ _y
(457) CH(457) CH
N— ^ ^— N (458) CHN— ^ ^ - N (458) CH
NC \ r- j (459) N- -N CHNC \ r- j (459) N- -N CH
N-"N ^ N - "N ^
(462) /=\_ CF3 CH (462) / = \ _ CF 3 CH
(464) ζr CF3 CH (464) CFr CF 3 CH
(465) N _ \_J~~ (465) N _ \ _J ~~
(466)(466)
F- - x N F - - x N
(467)(467)
\ N- y ' \ //\ N- y '\ //
(468)(468)
NC \\ y w //NC \\ y w //
(480) N (480) N
\__ ~ Q~ \ __ ~ Q ~
(481) N(481) N
F~C^ • Q~ F ~ C ^ • Q ~
(482) N(482) N
Q~~ Q~ Q ~~ Q ~
(483) N m- -(483) N m - -
(485)(485)
\-)~ -ö N\ -) ~ -ö N
(486)(486)
F~ ~ -ö N F ~ ~ -ö N
(487) CF3 N ~ (487) CF 3 N ~
(488) CF3 N(488) CF 3 N
Hc^ ~ Hc ^ ~
(489) CF3 N(489) CF 3 N
Beispiele 490 - 539:Examples 490-539:
R R2 XRR 2 X
(492) CH (492) CH
\ N // ' \ // ( 03)\ N // '\ // (03)
Nc C-)- CH Nc C -) - CH
XXXX
(494) CH(494) CH
N X~ XXNX ~ XX
(506) CH(506) CH
F_ _ Q~ F_ _ Q ~
(507) y=v /^x CH ^ ^(507) y = v / ^ x CH ^ ^
(508) CH(508) CH
NC_^- Q~ NC_ ^ - Q ~
510) θ CH x, y510) θ CH x, y
511 CH511 CH
\\ //\\ //
512 CF3 CH512 CF 3 CH
\ *\ *
513 CF3 CH513 CF 3 CH
NC " //NC " //
514 ^ CF3 CH514 ^ CF 3 CH
515 N515 N
\\ // XJ\\ // XJ
(531) ==\ =\ N(531) == \ = \ N
\ // X "\ // X "
(532) ==\ /=\ N(532) == \ / = \ N
(533) /=\ =\ N(533) / = \ = \ N
NC-NC
(534) N-N. /=\ N ll /) — (\ /)— ■ (534) N -N. / = \ N ll /) - (\ /) - ■
(535) /=\ ^o N y~ Λ(535) / = \ ^ o N y ~ Λ
(536) /=\ o N(536) / = \ o N
F _ ~ U F _ ~ U
(537) /=\ CF3 N(537) / = \ CF 3 N
(539) ^ ^ CF3 N(539) ^ ^ CF 3 N
Beispiele 540 - 589: Examples 540 - 589:
R1 R2 54ÖT "CfR 1 R 2 54ÖT " Cf
\\ y \J\\ y \ J
(557) CH (557) CH
\ * V* (558) CH\ * V * (558) CH
NC- X\ // X -N / NC- X \ // X -N /
(562) CF3 CH (562) CF 3 CH
\ N // '\ N // '
(564) CF3 CH (564) CF 3 CH
(581) . =\ /==\ N(581) . = \ / == \ N
(583) /== /== N(583) / == / == N
NC- VT" *NC-VT " *
(584) • N-N == N(584) • N -N == N
N N-N X~ X ^ X~ N N -NX ~ X ^ X ~
(585) /=\ ^o N y~ J 74(585) / = \ ^ o N y ~ J 74
(586)(586)
F-0- -ϋ N F -0- -ϋ N
(588) CF3 N(588) CF 3 N
NC~0~ NC ~ 0 ~
(589) yy^ CF3 N(589) yy ^ CF 3 N
Beispiele 590 - 639:Examples 590 - 639:
R1 R2 XR 1 R 2 X
(590) CH(590) CH
G^~ \_IG ^ ~ \ _I
(591) CH(591) CH
F~ ~ \__J F ~ ~ \ __ J
(593) CH(593) CH
NC~0~ X_J NC ~ 0 ~ X_J
(606) =\ ' =\ CH(606) = \ ' = \ CH
(607) /=\ /== CH(607) / = \ / == CH
\ N- —X ' ~ x ^— N*\ N- —X ' ~ x ^ - N *
(610) =v o CH(610) = from CH
{_}- \J{_} - \ J
(612) /=\ CF3 CH(612) / = \ CF 3 CH
W ff n—vW ff n — v
(614) ϋr CF3 CH (614) CFr CF 3 CH
(615) N X χ_j—(615) N X χ_j—
(616) N(616) N
F_\y- X_J~ F_ \ y- X_J ~
(617) N ~ χ ~ (617) N ~ χ ~
(618) N C→Q- _(618) N C → Q- _
(619) N(619) N
II /) —II /) -
X__X__
(630) N ~J (630) N ~ J
(631) Q~ (631) Q ~
NN
F-Q- • C " F -Q- • C "
(632) N(632) N
Q~ Q~ Q ~ Q ~
(633) N(633) N
NC→Q- NC → Q-
(634) Q~ (634) Q ~
NN
V N - N ff~ V N - N ff ~
(635)(635)
G^~" -ö NG ^ ~ " -ö N
(636)(636)
F_G^" -ό N F_ G ^ " -ό N
(637) CF3 N(637) CF 3 N
Q~ Q ~
(638) CF3 N m^O~ (638) CF 3 N m ^ O ~
(639) <sx^ CF3 N(639) <sx ^ CF 3 N
Beispiele 640 - 689:Examples 640 - 689:
R1 R2 XR 1 R 2 X
(640) CH x_x \_}~ (640) CH x_x \ _} ~
(641) CH(641) CH
\__ ~ \ __ ~
(642) CH (642) CH
(656) CH(656) CH
F~ ~ Q~ F ~ ~ Q ~
(657) CH(657) CH
Q~ Q ~
(658) CH °^~)~ C (659) CH ιι )> —(658) CH ° ^ ~ ) ~ C (659) CH ιι)> -
N-N^ ^ N -N ^ ^
(660) CH(660) CH
\ ~ ■ -ö\ ~ ■ -ö
(661)(661)
F-0~ - CH F- 0 ~ - CH
(662) CF3 CH ~ (662) CF 3 CH ~
(663) CF3 CH(663) CF 3 CH
NC~0~ NC ~ 0 ~
(664)(664)
Or CF3 CH oOr CF 3 CH o
(665) N __J~ -G^~ (665) N __J ~ -G ^ ~
(666) ^o- N(666) ^ o- N
G^G ^
(667) N(667) N
Q~- G^~ Q ~ - G ^ ~
(668) N(668) N
NC~0~ G~ NC ~ 0 ~ G ~
(681) N(681) N
F~G^ ~ F ~ G ^ ~
(684) N(684) N
II > Q~ II> Q ~
(685)(685)
G^ -ö NG ^ -ö N
(686) -o -ö N(686) -o -ö N
(687) 0^ CF3 N(687) 0 ^ CF 3 N
(688)(688)
N°- - CF3 N N ° - - CF 3 N
(689) r CF3 N(689) r CF 3 N
Beispiele 690 - 739: Examples 690 - 739:
R1 R2 R 1 R 2
(690) CH(690) CH
X_J X_IX_J X_I
(693) CH(693) CH
NMG~ \_J N MG ~ \ _J
(694) CH(694) CH
XX
(710) CH(710) CH
-y>-y>
(711)(711)
F~ " -Φ CH F ~ " -Φ CH
(714) Cr CF3 CH(714) Cr CF 3 CH
(715) N(715) N
XJ XJXJ XJ
(716) N(716) N
F_ ^ F_ ^
(717) N(717) N
(G~ J(G ~ J
(718) N(718) N
Nc-G^ XX Nc -G ^ XX
(731) N(731) N
F-0~~ Q~ F -0 ~~ Q ~
(733) N(733) N
NCHG~ Q~ NC HG ~ Q ~
(734) N(734) N
N // " Q~ N // " Q ~
(735) N(735) N
4 "" -ö (736) 0-, // u N4 "" -ö (736) 0-, // u N
(737) CF3 (737) CF 3
\ N- // ' (738)\ N- // '(738)
NC- CF3 NC CF 3
X\ //X \ //
Beispiele 740 - 789:Examples 740 - 789:
R1 R2 XR 1 R 2 X
(741) CH(741) CH
F~G^~ J F ~ G ^ ~ J
(742) CH(742) CH
Q~ XJQ ~ XJ
(743) CH(743) CH
NcG ~ Nc G ~
(757) /=\ /=\ CH(757) / = \ / = \ CH
X N— / V/ X X^-M ttX N— / V / X X ^ -M tt
(759) N-N /== CH(759) N -N / == CH
(761) _/=\_ ^°\ CH(761) _ / = \ _ ^ ° \ CH
(762) =\ CF3 CH(762) = \ CF 3 CH
X*X *
(763) =\ CF3 CH(763) = \ CF 3 CH
NC ;^x y NC ; ^ xy
(767) =\ N(767) = \ N
\ N—V ff \_y\ N — V ff \ _y
(780) N ff -N (781) N x // x -N (782) (780) N ff -N (781) N x // x -N (782)
X * x -N (783) NX * x -N (783) N
NC- X\ // N. -N / (784)NC-X \ // N. -N / (784)
N ^N ^
N -N (785) N y N -N (785) Ny
(787) CF3 N (787) CF 3 N
X * (788) CF3 NX * (788) CF 3 N
NC- XX //NC- XX //
Beispiele 790 - 839:Examples 790 - 839:
R R2 XRR 2 X
(790) CH ff XJ(790) CH ff XJ
(791) CH(791) CH
F"X\ // X // (792) CH F " X \ // X // (792) CH
G~ G-G ~ G-
(794) CH(794) CH
II /) — -II /) - -
(806) CH(806) CH
F~0~ Q~ F ~ 0 ~ Q ~
(807) CH(807) CH
Q~~ Q~ (808) CHQ ~~ Q ~ (808) CH
NC- // x -N (809) CHNC- // x -N (809) CH
IN^N x -N (810) CHIN ^ N x -N (810) CH
\\ (811) CH ~ y w // (812) CF3 CH\\ (811) CH ~ yw // (812) CF 3 CH
N ' (813) CF3 CHN '(813) CF 3 CH
NC-^ /r NC- ^ / r
(815) N x (815) N x
(835)(835)
G^~ -ö NG ^ ~ -ö N
(836)(836)
F-^G~ X) N F - ^ G ~ X) N
(837) CF3 N(837) CF 3 N
Q~ Q ~
(838) CF3 N(838) CF 3 N
NC-0~ NC -0 ~
(839) Cr CF3 N(839) Cr CF 3 N
Beispiele 840 - 889: Examples 840 - 889:
R1 R2 XR 1 R 2 X
(840)(840)
G^ CHG ^ CH
G~ G ~
(841) CH θ- J(841) CH θ- J
(842) CH(842) CH
Q~ JQ ~ J
(843) CH(843) CH
NC — .NC -.
XJXJ
(844) CH(844) CH
N // JN // Y
(860)(860)
G~ X) CHG ~ X) CH
(861)(861)
FG ~ X) CH F G ~ X) CH
0 (862)0 (862)
0~ CF3 CH0 ~ CF 3 CH
(863) CF3 CH m-ζ ~ (863) CF 3 CH m -ζ ~
(864) 5 Cr CF3 CH(864) 5 Cr CF 3 CH
(865) N(865) N
G^~ XJG ^ ~ XJ
0 (867) N 0 (867) N
Q~ X_Q ~ X_
(868) N(868) N
HC~ ^ — XJ HC ~ ^ - XJ
(869) N o N X~ XJ (869) N o NX ~ XJ
(881) /=\ /=\ N(881) / = \ / = \ N
FF
(883) NC_ =\ =\ N w " \\(883) NC _ = \ = \ N w " \\
(885) ==\ ^-o N (885) == \ ^ -o N
(887) ~ CF3 N(887) ~ CF 3 N
(888) CF3 N n°-{~ ~ (888) CF 3 N n ° - { ~ ~
(889) er CF3 N(889) he CF 3 N
Beispiele 89 - 1059:Examples 89 - 1059:
HT2A IC50 HT2C IC50HT2A IC50 HT2C IC50
(890) {2-[1-(4'-Fluor-biphenyl-4-yl)-5-(2-fluor- 1.50E-09 2,74E-08 phenyl)-1 H-pyrazol-4-yl]-ethyl}-dimethyl-amin(890) {2- [1- (4'-fluoro-biphenyl-4-yl) -5- (2-fluoro-1.50E-09 2.74E-08 phenyl) -1 H-pyrazol-4-yl] -ethyl} -dimethyl-amine
(891) 1-[5-Furan-2-yl-1-(4-thiophen-3-yl-phenyl)-1 H- 4.50E-09 2.10E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin(891) 1- [5-furan-2-yl-1- (4-thiophene-3-yl-phenyl) -1 H- 4.50E-09 2.10E-07 pyrazol-4-ylmethyl] -4-methyl- piperazine
(892) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 5.20E-09 4,20E-07 pyrazol-4-ylmethyl]-amino}-ethanol(892) 2 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 5.20E-09 4.20E-07 pyrazol-4-ylmethyl] amino} ethanol
(893) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 6.40E-09 2.30E-07 pyrazol-4-ylmethyl]-4-methyl-[1,43diazepam(893) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 6.40E-09 2.30E-07 pyrazol-4-ylmethyl] -4-methyl- [1,43diazepam
(894) N-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 6.50E-09 4.50E-07 pyrazol-4-ylmethyl]-ethan-1 ,2-diamin(894) N- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 6.50E-09 4.50E-07 pyrazol-4-ylmethyl] ethane-1,2-diamine
(895) 1-[5-(2-Fluor-phenyl)-1-(4'-methoxy-biphenyl- 7,50E-09 1.15E-06 4-yl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(895) 1- [5- (2-fluorophenyl) -1- (4'-methoxy-biphenyl- 7.50E-09 1.15E-06 4-yl) -1 H-pyrazol-4-ylmethyl] - 4-methylpiperazine
(896) 4-[5-(2-Fluor-phenyl)-1-(4-trifluormethyl- 8,00E-09 4.30E-05 phenyl)-1 H-pyrazol-4-ylmethyl]-piperazin-1 - carbonsäuretert-butyl ester (897) [1-Biphenyl-4-yI-5-(2-fluor-phenyl)-1 H- 1 ,10E-08 1 ,00E-06 pyrazol-4-ylmethyl]-diethyl-amin(896) 4- [5- (2-Fluorophenyl) -1- (4-trifluoromethyl-8.00E-09 4.30E-05 phenyl) -1 H-pyrazol-4-ylmethyl] piperazin-1 - carboxylic acid tared -butyl ester (897) [1-Biphenyl-4-yI-5- (2-fluorophenyl) -1 H-1, 10E-08 1,00E-06 pyrazol-4-ylmethyl] diethylamine
(898) 4-{2-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1.20E-08 1.00E-06 pyrazol-4-yl3-ethyl}-morpholin(898) 4- {2- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1.20E-08 1.00E-06 pyrazol-4-yl3-ethyl} morpholine
(899) 1-{1-[4-(2,3-Dihydro-benzo[1 ,4]dioxin-6-yl)- 1.20E-08 n.d. phenyl3-5-phenyl-1 H-pyrazol-4-yl}-4-methyl- piperazin(899) 1- {1- [4- (2,3-Dihydro-benzo [1,4] dioxin-6-yl) -1.20E-08 n.d. phenyl3-5-phenyl-1H-pyrazol-4-yl} -4-methylpiperazine
(900) 1-[1-(4'-Fluor-biphenyl-4-yl)-5-phenyl-1H- 1 ,30E-08 3.10E-07 pyrazoi-4-ylmethyl]-4-methyl-piperazin(900) 1- [1- (4'-Fluoro-biphenyl-4-yl) -5-phenyl-1H-1, 30E-08 3.10E-07 pyrazoi-4-ylmethyl] -4-methyl-piperazine
(901) 1-[1-[4-(2,3-Dihydro-benzo[1 ,4]dioxin-6-yl)- 1.30E-08 8.70E-07 phenyl3-5-(2-fluor-phenyl)-1 H-pyrazol-4- ylmethyl]-4-methyl-piperazin(901) 1- [1- [4- (2,3-Dihydro-benzo [1,4] dioxin-6-yl) - 1.30E-08 8.70E-07 phenyl3-5- (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(902) 1-[1-(4*-Fluor-biphenyl-4-yl)-5-(2-fluor-phenyl)- 1.31E-08 2.15E-07 1 H-pyrazol-4-ylmethyl]-4-methyl-piperazin(902) 1- [1- (4 * -fluorobiphenyl-4-yl) -5- (2-fluorophenyl) - 1.31E-08 2.15E-07 1 H-pyrazol-4-ylmethyl] -4 -methyl-piperazine
(903) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1.40E-08 4.70E-07 pyrazol-4-ylmethyl]-(4-methyl-piperazin-1-yl)- amin(903) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1.40E-08 4.70E-07 pyrazol-4-ylmethyl] - (4-methyl-piperazin-1-yl ) - amine
(904) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1 ,40E-08 2,00E-06 pyrazol-4-ylmethyl]-pyrrolidin-3-ol(904) 1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-1,40E-08 2.00E-06 pyrazol-4-ylmethyl] pyrrolidin-3-ol
(905) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1 ,60E-08 1.00E-06 pyrazol-4-ylmethyl]-(2-methoxy-ethyl)-amin(905) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1, 60E-08 1.00E-06 pyrazol-4-ylmethyl] - (2-methoxy-ethyl) amine
(906) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.60E-08 1.00E-06 pyrazol-4-ylmethyl]-methyl-amino}-ethanol(906) 2 - {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H-1.60E-08 1.00E-06 pyrazol-4-ylmethyl] methylamino} ethanol
(907) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1 ,60E-08 8,40E-08 py razol-4-ylmethyl]-methyl-( 1 -methyl- pyrrolidin-3-yl)-amin (908) 4-{3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.70E-08 n.d. pyra∑ol-4-yl3-allyl}-morpholin(907) [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-1, 60E-08 8.40E-08 pyrazol-4-ylmethyl] methyl- (1-methyl- pyrrolidin-3-yl) -amine (908) 4- {3- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H-1.70E-08 and pyra∑ol-4-yl3-allyl} morpholine
(909) 1-[5-(2-Fluor-phenyl)-1-(4-pyrrol-1-yl-phenyl)- 1.70E-08 2,10E-07 1 H-pyrazoI-4-ylmethyl]-4-methyl-piperazin(909) 1- [5- (2-fluorophenyl) -1- (4-pyrrol-1-ylphenyl) - 1.70E-08 2,10E-07 1 H-pyrazoI-4-ylmethyl] -4 -methyl-piperazine
(910) 1-[1-(4'-Methoxy-biphenyl-4-yl)-5-phenyl-1 H- 1.80E-08 n.d. pyrazol-4-yl]-4-methyl-piperazin(910) 1- [1- (4'-Methoxy-biphenyl-4-yl) -5-phenyl-1 H-1.80E-08 n.d. pyrazol-4-yl] -4-methyl-piperazine
(911) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-(3-fluorphenyl)- 1.90E-08 n.d. 1 H-pyrazol-4-ylmethylj-4-methylpiperazin(911) 1- [1- (4'-fluorobiphenyl-4-yl) -5- (3-fluorophenyl) - 1.90E-08 n.d. 1 H-pyrazol-4-ylmethylj-4-methylpiperazine
(912) N-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2,00E-08 9.20E-07 pyrazol-4-ylmethyl3-N,N',N'-trimethyl-ethan-(912) N- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.00E-08 9.20E-07 pyrazol-4-ylmethyl3-N, N ', N'-trimethyl ethane
1 ,2-diamin1, 2-diamine
(913) 1-{2-[1-(4'-Fluor-biphenyl-4-yl)-5-(2-fluor- 2.00E-08 6,20E-07 phenyl)-1H-pyrazol-4-yl3-ethyl}-pyrrolidin-3-ol(913) 1- {2- [1- (4'-Fluoro-biphenyl-4-yl) -5- (2-fluoro-2.00E-08 6.20E-07 phenyl) -1H-pyrazol-4-yl3 ethyl} -pyrrolidin-3-ol
(914) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.10E-08 4.50E-07 pyrazol-4-ylmethylJ-dimethyl-amin(914) [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.10E-08 4.50E-07 pyrazol-4-ylmethylJ-dimethyl-amine
(915) C-(1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-yl)- 2.10E-08 9.20E-07 methylamin(915) C- (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4-yl) -2.10E-08 9.20E-07 methylamine
(916) 1-[5-(2-Fluor-phenyl)-1-(4'-methyl-biphenyl-4- 2.20E-08 9.60E-07 yl)-1 H-pyrazol-4-ylmethyl3-4-methyl-piperazin(916) 1- [5- (2-fluorophenyl) -1- (4'-methyl-biphenyl-4- 2.20E-08 9.60E-07 yl) -1 H-pyrazol-4-ylmethyl3-4- methyl-piperazine
(917) 4-{3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.30E-08 n.d. pyrazol-4-yl]-propyl}-morpholin(917) 4- {3- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 2.30E-08 n.d. pyrazol-4-yl] -propyl} -morpholine
(918) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazot-4- 2.30E-08 1.00E-06 ylmethyl)-pyridin-2-ylmethyl-amin(918) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazot-4- 2.30E-08 1.00E-06 ylmethyl) pyridin-2-ylmethylamine
(919) 1-[2-(2,4-Difluor-phenyl)-ethyl3-4-[5-(2-fluor- ' 2,30E-08 1.00E-06 phenyl)-1 -pyridin-2-yl-1 H-pyrazol-4-ylmethyl]- piperazin(919) 1- [2- (2,4-difluorophenyl) ethyl3-4- [5- (2-fluoro- ' 2.30E-08 1.00E-06 phenyl) -1-pyridin-2-yl-1 H-pyrazol-4-ylmethyl] piperazine
(920) 1-[1-(4'-Chlor-biphenyl-4-yl)-5-(2-fIuor- 2.30E-08 3.30E-07 phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(920) 1- [1- (4'-Chlorobiphenyl-4-yl) -5- (2-fluorine-2.30E-08 3.30E-07 phenyl) -1 H -pyrazol-4-ylmethyl] -4 -methyl piperazine
(921) 1-{2-[1-(4'-Fluor-biphenyl-4-yl)-5-(2-fluor- 2,33E-08 7.30E-07 phenyl)-1 H-pyrazol-4-yl]-ethyl}-4-methyl- piperazin(921) 1- {2- [1- (4'-Fluoro-biphenyl-4-yl) -5- (2-fluoro-2,33E-08 7.30E-07 phenyl) -1 H-pyrazole-4- yl] -ethyl} -4-methyl-piperazine
(922) 1-[5-(2-Fluor-phenyl)-1-(5-phenyl-pyridin-2- 2,40E-08 6,60E-07 yl)-1 H-pyrazol-4-ylmethyl3-4-methyl-piperazin(922) 1- [5- (2-Fluoro-phenyl) -1- (5-phenyl-pyridine-2- 2.40E-08 6.60E-07 yl) -1 H-pyrazol-4-ylmethyl3-4 -methyl-piperazine
(923) 1-[1-(4'-Fluor-biphenyl-4-yl)-5-(4-fluor-phenyl)- 2,50E-08 7.50E-07(923) 1- [1- (4'-Fluoro-biphenyl-4-yl) -5- (4-fluoro-phenyl) - 2.50E-08 7.50E-07
1 H-pyrazol-4-ylmethyl]-4-methyl-piperazin1 H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(924) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.60E-08 6,60E-07 pyrazol-4-ylmethyl]-piperazin(924) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.60E-08 6.60E-07 pyrazol-4-ylmethyl] piperazine
(925) (1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4- 2.60E-08 5.20E-07 ylmethyl)-(1 -methyl-1 H-pyrrol-2-ylmethyl)- amin(925) (1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4- 2.60E-08 5.20E-07 ylmethyl) - (1-methyl-1 H-pyrrol-2-ylmethyl) amine
(926) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2,73E-08 6.00E-07 pyrazol-4-ylmethyl]-4-methyl-piperazin(926) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.73E-08 6.00E-07 pyrazol-4-ylmethyl] -4-methyl-piperazine
(927) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.80E-08 1.00E-06 pyrazol-4-ylmethylj-4-ethyl-piperazin(927) 1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-2.80E-08 1.00E-06 pyrazol-4-ylmethylj-4-ethyl-piperazine
(928) 1-Ethyl-4-{2-[1-(4'-fluor-biphenyl-4-yl)-5-(2- 2.80E-08 1.30E-06 fluor-phenyl)-1H-pyrazol-4-yl]-ethyl}-piperazin(928) 1-Ethyl-4- {2- [1- (4'-fluoro-biphenyl-4-yl) -5- (2- 2.80E-08 1.30E-06 fluoro-phenyl) -1H-pyrazole- 4-yl] -ethyl} -piperazine
(929) N-{1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2,90E-08 1.00E-06 pyrazol-4-ylmethyl]-pyrrolidin-3-yl}-acetamid (930) 1-[5-(2-Fluor-phenyl)-1-(3*-methoxy-biphenyl- 2,90E-08 6.90E-07 4-y I)- 1 H-pyrazol-4-ylmethyl]-4-methy I- pipera∑in(929) N- {1- [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H- 2.90E-08 1.00E-06 pyrazol-4-ylmethyl] pyrrolidin-3- yl} -acetamide (930) 1- [5- (2-fluorophenyl) -1- (3 * -methoxy-biphenyl-2.90E-08 6.90E-07 4-y I) - 1 H-pyrazol-4-ylmethyl] -4-methy I-pipera∑in
(931) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3,00E-08 1.00E-06 pyra∑ol-4-ylmethyl]-piperidin(931) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.00E-08 1.00E-06 pyra∑ol-4-ylmethyl] piperidine
(932) (1-Biphenyl-4-yl-5-phenyl-1H-pyra∑ol-4- 3.10E-08 1 ,00E-06 ylmethyl)-pyridin-4-ylmethyl-amin(932) (1-Biphenyl-4-yl-5-phenyl-1H-pyra∑ol-4- 3.10E-08 1, 00E-06 ylmethyl) -pyridin-4-ylmethyl-amine
(933) [5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 3.10E-08 1.00E-06 1 H-pyrazol-4-yI]-methanol(933) [5- (4-Chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) -3.10E-08 1.00E-06 1 H-pyrazol-4-yI] methanol
(934) 1-Biphenyl-4-yl-5-(2-fluor-phenyl)-4-pyrrolidin- 3,20E-08 1 ,00E-06 1-ylmethyl-1 H-pyrazole(934) 1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -4-pyrrolidine-3.20E-08 1, 00E-06 1-ylmethyl-1 H-pyrazole
(935) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 3.40E-08 1.00E-06 pyrazol-4-ylmethyl]-(3-methoxy-propyI)-amin(935) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-3.40E-08 1.00E-06 pyrazol-4-ylmethyl] - (3-methoxypropyl) amine
(936) {1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 3.50E-08 n.d. pyrazol-4-ylmethyl]-pyrrolidin-3-yl}-dimethyl- amin(936) {1- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-3.50E-08 n.d. pyrazol-4-ylmethyl] pyrrolidin-3-yl} dimethyl amine
(937) [5-(2-Fluor-phenyl)-1-(5-trifluormethyl-pyridin- 3.50E-08 1.00E-06 2-yl)-1 H-pyrazol-4-ylmethyl3-dimethyl-amin(937) [5- (2-fluorophenyl) -1- (5-trifluoromethyl-pyridine-3.50E-08 1.00E-06 2-yl) -1 H-pyrazol-4-ylmethyl3-dimethyl-amine
(938) 1-Ethyl-4-[1-(4'-fluorbiphenyl-4-yl)-5-(3- 3.50E-08 n.d. methoxyphenyl)-1H-pyrazol-4-ylmethyl]- piperazin(938) 1-Ethyl-4- [1- (4'-fluorobiphenyl-4-yl) -5- (3- 3.50E-08 n.d methoxyphenyl) -1H-pyrazol-4-ylmethyl] piperazine
(939) 1-Biphenyl-4-yl-4-(2,5-dihydro-pyrrol-1- 3,60E-08 n.d. ylmethyl)-5-(2-fluor-phenyl)-1 H-pyrazole(939) 1-Biphenyl-4-yl-4- (2,5-dihydro-pyrrol-1 - 3.60E-08 n.d. ylmethyl) -5- (2-fluorophenyl) -1 H-pyrazole
(940) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-m-tolyl-1H- 3.70E-08 n.d. pyrazol-4-ylmethyl3-4-methylpiperazin (941) 1-[5-(2-Fluor-phenyl)-1-(5-trifluormethyl- 3.90E-08 1,O0E-06 pyridin-2-yl)-1H-pyrazol-4-ylmethyl]-4-methyl- piperazin(940) 1- [1- (4'-Fluorobiphenyl-4-yl) -5-m-tolyl-1H-3.70E-08 and pyrazol-4-ylmethyl3-4-methylpiperazine (941) 1- [5- (2-fluorophenyl) -1- (5-trifluoromethyl-3.90E-08 1, O0E-06 pyridin-2-yl) -1H-pyrazol-4-ylmethyl] -4- methyl piperazine
(942) (1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4- 3.90E-08 1.00E-06 ylmethyl)-(1 -methyl-1 H-imidazol-2-ylmethyl)- amin(942) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4- 3.90E-08 1.00E-06 ylmethyl) - (1-methyl-1H-imidazol-2-ylmethyl) amine
(943) 1-[5-(3-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 4.10E-08 1,00E-06 1 H-pyrazol-4-ylmethyl]-4-isopropyIpiperazin(943) 1- [5- (3-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 4.10E-08 1.00E-06 1 H-pyrazol-4-ylmethyl] -4-isopropylipiperazine
(944) 1-[5-(2-Fluor-phenyl)-1-(4-trifluormethyl- 4.30E-08 7.90E-07 phenyl)-1H-pyrazol-4-ylmethyl]-piperazin(944) 1- [5- (2-Fluorophenyl) -1- (4-trifluoromethyl-4.30E-08 7.90E-07 phenyl) -1H-pyrazol-4-ylmethyl] piperazine
(945) 4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 4,30E-08 1.00E-06 pyrazol-4-ylmethyl]-thiomorpholin 1 ,1-dioxid(945) 4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 4.30E-08 1.00E-06 pyrazol-4-ylmethyl] thiomorpholine 1, 1-dioxide
(946) N-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 4,40E-08 4.90E-07 1H-pyrazol-4-ylmethyl]-N,N',N'-trimethylethan- 1,2-diamin(946) N- [5- (2-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 4.40E-08 4.90E-07 1H-pyrazol-4-ylmethyl] -N, N ', N'-trimethylethane-1,2-diamine
(947) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 4.69E-08 1.00E-06 pyrazol-4-ylmethylj-(1-ethyl-pyrrolidin-2- ylmethyl)-amin(947) [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 4.69E-08 1.00E-06 pyrazol-4-ylmethylj- (1-ethyl-pyrrolidin-2-ylmethyl) amine
(948) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 4.80E-08 n.d. pyrazol-4-ylmethyl]-azepan(948) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 4.80E-08 n.d. pyrazol-4-ylmethyl] -azepane
(949) 1-(1-Biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4- 5.00E-08 1.00E-06 ylmethyl)-4-methyl-piperazin(949) 1- (1-Biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4- 5.00E-08 1.00E-06 ylmethyl) -4-methyl-piperazine
(950) 1-[2-(4-Fluor-phenyl)-ethyl]-4-[5-(2-fluor- 5.30E-08 n.d. phenyl)-1-pyridin-2-yl-1H-pyrazol-4-ylmethyl]- piperazin(950) 1- [2- (4-fluorophenyl) ethyl] -4- [5- (2-fluoro-5.30E-08 nd phenyl) -1-pyridin-2-yl-1H-pyrazol-4 -ylmethyl] - piperazine
(951) [5-(2-Chlorphenyl)-1-(4,-fluorbiphenyl-4-yl)- 5.30E-08 1.00E-06 1 H-pyrazol-4-ylmethy l]-d iethylam i n(951) [5- (2-chlorophenyl) -1- (4 , -fluorobiphenyl-4-yl) - 5.30E-08 1.00E-06 1 H-pyrazol-4-ylmethyl] -d-ethylam in
(952) 4'-[5-(2-Fluor-phenyl)-4-(4-methyl-piperazin-1- 5.30E-08 7,90E-07 ylmethyl)-pyrazol-1-yl]-biphenyl-4-carbonitril(952) 4 '- [5- (2-fluorophenyl) -4- (4-methyl-piperazin-1- 5.30E-08 7.90E-07 ylmethyl) -pyrazol-1-yl] -biphenyl-4 carbonitrile
(953) l-fl^'.S'-Difluor-biphenyM-yö-S^-fluor- 5,50E-08 4.70E-07 phenyl)-1H-pyrazol-4-ylmβthylj-4-methyl- pipera∑in(953) l-fl ^ '. S'-difluoro-biphenyM-yö-S ^ -fluor- 5.50E-08 4.70E-07 phenyl) -1H-pyrazol-4-ylmβthylj-4-methylpiperaiperin
(954) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-(4- 5.60E-08 n.d. methoxyphenyl)-1H-pyrazol-4-ylmethyl3-4-(2- pyrrolidin-1 -yl-ethyl)-piperazin(954) 1- [1- (4'-Fluorobiphenyl-4-yl) -5- (4- 5.60E-08 and methoxyphenyl) -1H-pyrazol-4-ylmethyl3-4- (2-pyrrolidin-1-yl ethyl) piperazine
(955) 1-[1-(2,,4'-Difluor-biphenyl-4-yl)-5-(2-fluor- 5,60E-08 n.d. phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(955) 1- [1- (2, 4'-difluoro-biphenyl-4-yl) -5- (2-fluoro-5,60E-08 nd phenyl) -1 H-pyrazol-4-ylmethyl] - 4-methylpiperazine
(956) 1-[1-(4'-Ethyl-biphenyl-4-yl)-5-(2-fluor-phenyl)- 5.70E-08 n.d. 1H-pyrazol-4-ylmethyl]-4-methyl-piperazin(956) 1- [1- (4'-Ethylbiphenyl-4-yl) -5- (2-fluorophenyl) - 5.70E-08 n.d. 1H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(957) 4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 5.80E-08 n.d. pyrazol-4-ylmethyl]-piperazin-1- carbonsäureethyl ester(957) 4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 5.80E-08 n.d. pyrazol-4-ylmethyl] piperazin-1-carboxylic acid ethyl ester
(958) 1-[5-(2-Fluor-phenyl)-1-(4'-isopropyl-biphenyl- 5,81 E-08 8,30E-07(958) 1- [5- (2-fluorophenyl) -1- (4'-isopropyl-biphenyl-5.81 E-08 8.30E-07
4-yl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin4-yl) -1 H-pyrazol-4-ylmethyl] -4-methylpiperazine
(959) l-fl^'.S'-Difluor^'-methyl-biphenyM-y -δ- 6,00E-08 n.d. (2-fluor-phenyl)-1 H-pyrazol-4-ylmethyl]-4- methyl-piperazin(959) l-fl ^ '. S'-difluoro ^' - methyl-biphenyM-y -δ- 6.00E-08 n.d. (2-fluorophenyl) -1 H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(960) 1-[1-(3',4'-Difluor-biphenyl-4-yl)-5-(2-fluor- 6,00E-08 3,40E-07 phenyl)-1H-pyrazol-4-ylmethyI]-4-methyl- pipera∑in (961) 1-(3-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 6.40E-08 1 ,00E-06 pyrazol-4-ylmethyl]-amino}-propyl)-pyrrolidin- 2-on(960) 1- [1- (3 ', 4'-difluorobiphenyl-4-yl) -5- (2-fluoro-6.00E-08 3.40E-07 phenyl) -1H-pyrazole-4- ylmethyI] -4-methylpipera∑in (961) 1- (3 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 6.40E-08 1, 00E-06 pyrazol-4-ylmethyl] -amino} - propyl) pyrrolidin-2-one
(962) 3-{1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 6,60E-08 n.d. pyrazol-4-ylmethyi]-piperidin-4-ylmethyl}- pyridin(962) 3- {1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 6.60E-08 n.d. pyrazol-4-ylmethyi] piperidin-4-ylmethyl} pyridine
(963) 1-[1-(3*-Chlor-biphenyl-4-yl)-5-(2-fluor- 6.90E-08 n.d. o phenyl)-1 H-pyrazol-4-ylmethyl}-4-methyl- piperazin(963) 1- [1- (3 * chlorobiphenyl-4-yl) -5- (2-fluoro-6.90E-08 and o-phenyl) -1 H-pyrazol-4-ylmethyl} -4-methyl - piperazine
(964) 2-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 7,00E-08 1 ,0OE-O6 pyrazol-4-ylmethyl3-1 ,2,3,4-tetrahydro- 5 isochinolin(964) 2- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 7.00E-08 1, 0OE-O6 pyrazol-4-ylmethyl3-1, 2,3,4 -tetrahydro- 5 isoquinoline
(965) 1-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 7.20E-08 6.00E-07 1 H-pyrazol-4-ylmethyl]-4-methylpiperazin(965) 1- [5- (2-Chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 7.20E-08 6.00E-07 1 H-pyrazol-4-ylmethyl] -4-methylpiperazine
0 (966) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-o-tolyl-1 H- 7.20E-08 n.d. pyrazol-4-ylmethyl3-4-methylpiperazin0 (966) 1- [1- (4'-fluorobiphenyl-4-yl) -5-o-tolyl-1 H- 7.20E-08 n.d. pyrazol-4-ylmethyl3-4-methylpiperazine
(967) 1-[1-(2',3'-Difluor-biphenyl-4-yl)-5-(2-fluor- 7,30E-08 n.d. phenyl)-1H-pyrazol-4-ylmethylJ-4-methyi- 5 . piperazin(967) 1- [1- (2 ', 3'-difluorobiphenyl-4-yl) -5- (2-fluoro-7.30E-08 and phenyl) -1H-pyrazol-4-ylmethylJ-4- methyi- 5. piperazine
(968) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 7.50E-08 n.d. pyrazol-4-ylmethyl3-4-pyridin-4-ylmethyl- piperazin 0(968) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 7.50E-08 n.d. pyrazol-4-ylmethyl3-4-pyridin-4-ylmethylpiperazine 0
(969) (1 H-Benzoimidazol-2-ylmethyl)-[1-biphenyl-4- 7,60E-08 1.00E-06 yl-5-(2-fluor-phenyl)-1H-pyrazol-4-ylmethyl]- amin(969) (1 H-benzoimidazol-2-ylmethyl) - [1-biphenyl-4- 7.60E-08 1.00E-06 yl-5- (2-fluorophenyl) -1H-pyrazol-4-ylmethyl] - amine
5 (970) {4'-[5-(2-Fluor-phenyl)-4-(4-methyl-piperazin- 8.10E-08 n.d.5 (970) {4 '- [5- (2-Fluoro-phenyl) -4- (4-methyl-piperazine-8.10E-08 n.d.
1 -ylmethyl)-pyrazol-1 -yl]-biphenyl-2-ylmethyl}- dim'ethyl-arriin1 -ylmethyl) -pyrazol-1 -yl] -biphenyl-2-ylmethyl} - dim'ethyl-arriin
(971 4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 8,20E-08 1.00E-06 pyrazol-4-ylmethyl]-piperazin-1- carb.onsäuretert-butyl ester(971 4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 8.20E-08 1.00E-06 pyrazol-4-ylmethyl] piperazin-1-carboxylic acid tert-butyl ester
(972) 2-[2-(4'-FIuorbiphenyl-4-yl)-4-(4- 8.50E-08 n.d. methylpiperazin-1-ylmethyl)-2H-pyrazol-3-yI3- pyrazin(972) 2- [2- (4'-Fuorbiphenyl-4-yl) -4- (4- 8.50E-08 n.d methylpiperazin-1-ylmethyl) -2H-pyrazol-3-yI3-pyrazine
(973) 1-[1-(3',5'-Dichlor-biphenyl-4-yl)-5-(2-fluor- 8,60E-08 n.d. phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(973) 1- [1- (3 ', 5'-dichlorobiphenyl-4-yl) -5- (2-fluoro-8.60E-08 and phenyl) -1 H-pyrazol-4-ylmethyl] - 4-methylpiperazine
(974) [1-(4,-Fluorbiphenyl-4-yl)-5-phenyl-1H- 8,70E-08 n.d. pyrazol-4-ylmethyl]-(4-methylpiperazin-1-yl)- amin(974) [1- (4 , -Fluorobiphenyl-4-yl) -5-phenyl-1H- 8.70E-08 and pyrazol-4-ylmethyl] - (4-methylpiperazin-1-yl) amine
(975) 1-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 8,80E-08 1.00E-06 1 H-pyrazol-4-ylmethyl]-4-ethylpiperazin(975) 1- [5- (2-Chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 8.80E-08 1.00E-06 1 H-pyrazol-4-ylmethyl] -4-ethylpiperazine
(976) 1-[1-(2'-Fluor-biphenyl-4-yl)-5-(2-fluor-phenyl)- 9.30E-08 3,71 E-07 1H-pyrazol-4-ylmethyl]-4-methyl-piperazin(976) 1- [1- (2'-fluoro-biphenyl-4-yl) -5- (2-fluoro-phenyl) - 9.30E-08 3.71 E-07 1H-pyrazol-4-ylmethyl] - 4-methyl-piperazine
(977) 2-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 9.40E-08 6.80E-07 py razol-4-ylmethyl3-5-methyl-2 , 5-d iaza- bicyclo[2.2.1]heptan(977) 2- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 9.40E-08 6.80E-07 py razol-4-ylmethyl3-5-methyl-2, 5-d iazabicyclo [2.2.1] heptane
(979) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.00E-07 n.d. pyrazol-4-ylmethyl]-3,5-dimethyl-piperazin (980) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1 ,00E-07 n.d. pyrazol-4-ylmethyl3-amino}-N-(4-nitro-phenyl)- acetamid(979) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H-1.00E-07 and pyrazol-4-ylmethyl] -3,5-dimethyl-piperazine (980) 2 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1H-1,00E-07 and pyrazol-4-ylmethyl3-amino} -N- (4-nitro-phenyl ) - acetamide
(981) 1-[1-(2*,5'-Difluor-biphenyl-4-yl)-5-phenyl-1H- 1,10E-07 1.00E-06 pyrazol-4-ylmethyl]-4-methyl-piperazin(981) 1- [1- (2 * , 5'-difluorobiphenyl-4-yl) -5-phenyl-1H-1.10E-07 1.00E-06 pyrazol-4-ylmethyl] -4-methyl- piperazine
(982) Cyclopropyl-bis-[1-(4'-fluor-biphenyl-4-yl)-5- 1.10E-07 n.d. furan-2-yl-1 H-pyrazol-4-ylmethylj-amin(982) Cyclopropyl-bis- [1- (4'-fluoro-biphenyl-4-yl) -5- 1.10E-07 n.d. furan-2-yl-1 H-pyrazol-4-ylmethylj-amine
(983) 1-[5-(2-Fluor-phenyl)-1-(4-isopropyl-phenyl)- 1 ,20E-07 5.20E-07. 1H-pyrazol-4-ylmethyl]-4-methyl-piperazin(983) 1- [5- (2-fluorophenyl) -1- (4-isopropylphenyl) - 1, 20E-07 5.20E-07. 1H-pyrazol-4-ylmethyl] -4-methyl-piperazine
(984) 1-[1-(2'-Chlor-biphenyl-4-yl)-5-(2-fluor- 1.20E-07 n.d. phenyl)-1 H-pyrazol-4-ylmethylJ-4-methyl- piperazin(984) 1- [1- (2'-Chloro-biphenyl-4-yl) -5- (2-fluoro-1.20E-07 n.d phenyl) -1 H-pyrazol-4-ylmethylJ-4-methylpiperazine
(985) 2-{4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.22E-07 n.d. pyrazol-4-ylmethyf]-piperazin-1 -yl}-1 - pyrrolidin-1-yl-ethanon(985) 2- {4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 1.22E-07 n.d. pyrazol-4-ylmethyf] piperazin-1-yl} -1 - pyrrolidin-1-yl-ethanone
(986) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.30E-07 n.d. pyrazol-4-ylmethyl]-4-methyl-piperidin(986) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 1.30E-07 n.d. pyrazol-4-ylmethyl] -4-methyl-piperidine
(987) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.30E-07 n.d. pyrazol-4-ylmethyl]-amino}-2-cyano-acetamid(987) 2 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1H-1.30E-07 n.d. pyrazol-4-ylmethyl] -amino} -2-cyano-acetamide
(988) N-{4'-[5-(2-Fluor-phenyl)-4-(4-methyl- 1,30E-07 n.d. - piperazin-1-ylmethyl)-pyrazol-1-ylj-biphenyl-3- yl}-acetamid(988) N- {4 '- [5- (2-fluorophenyl) -4- (4-methyl-1,30E-07 nd - piperazin-1-ylmethyl) pyrazol-1-ylj-biphenyl-3 - yl} -acetamide
(989) 1-[1-(4-Bromo-phenyl)-5-(2-fluor-phenyl)-1H- 1.30E-07 n.d. pyrazol-4-ylmethyl]-4-methyl-piperazin(989) 1- [1- (4-Bromo-phenyl) -5- (2-fluorophenyl) -1H- 1.30E-07 n.d. pyrazol-4-ylmethyl] -4-methyl-piperazine
(990) 1-[5-(2-Fluor-phenyl)-1-(4-trifluormethyl- 1.33E-07 4.90E-07 phenyl)-1H-pyrazol-4-yImethyl]-4-methyl- piperazin(990) 1- [5- (2-fluorophenyl) -1- (4-trifluoromethyl-1.33E-07 4.90E-07 phenyl) -1H-pyrazol-4-yImethyl] -4-methylpiperazine
(991) (1-A∑a-bicyclo[2.2.23oct-3-yl)-[1-biphenyl-4-yl- 1.40E-07 n.d. 5-(2-fluor-phenyl)-1 H-pyra∑ol-4-ylmethyl]- amin(991) (1-A∑a-bicyclo [2.2.23oct-3-yl) - [1-biphenyl-4-yl-1.40E-07 n.d. 5- (2-fluorophenyl) -1 H-pyra∑ol-4-ylmethyl] amine
(992) [5-(3-ChIorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 1.40E-07 n.d. 1 H-pyrazol-4-yl]-methanol(992) [5- (3-Chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 1.40E-07 n.d. 1 H-pyrazol-4-yl] methanol
(993) 4'-[5-(2-Fluor-phenyl)-4-(4-methyl-piperazin-1- 1.40E-07 n.d. ylmethyl)-pyrazol-1 -ylj-biphenyl-3-carbonitril(993) 4 '- [5- (2-Fluoro-phenyl) -4- (4-methyl-piperazin-1- 1.40E-07 n.d. ylmethyl) -pyrazole-1-ylj-biphenyl-3-carbonitrile
(994) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-p-tolyl-1H- 1.40E-07 n.d. pyrazol-4-ylmethyl3-4-methylpiperazin(994) 1- [1- (4'-fluorobiphenyl-4-yl) -5-p-tolyl-1H-1.40E-07 n.d. pyrazol-4-ylmethyl3-4-methylpiperazine
(995) [1-Biphenyl-4-yi-5-(2-fluor-phenyl)-1H- 1.60E-07 n.d. pyrazol-4-yImethyl]-methyl-(1-methyl- piperidin-4-yl)-amin(995) [1-Biphenyl-4-yi-5- (2-fluorophenyl) -1H- 1.60E-07 n.d. pyrazol-4-yImethyl] methyl- (1-methylpiperidin-4-yl) amine
(996) 5-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1.60E-07 n.d. pyrazol-4-ylmethyl]-2-oxa-5-aza- bicyclo[2.2.1]heptan(996) 5- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1.60E-07 n.d. pyrazol-4-ylmethyl] -2-oxa-5-azabicyclo [2.2.1] heptane
(997) 1-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 1.60E-07 1.00E-06(997) 1- [5- (2-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 1.60E-07 1.00E-06
1 H-pyrazol-4-ylmethyl]-4-isopropylpiperazin1 H-pyrazol-4-ylmethyl] -4-isopropylpiperazine
(998) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.70E-07 n.d. pyrazol-4-ylmethyl]-1,2,3,6-tetrahydro-pyridin(998) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 1.70E-07 n.d. pyrazol-4-ylmethyl] -1,2,3,6-tetrahydro-pyridine
(999) 4-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 1.70E-07 n.d. pyrazol-4-ylmethyl]-methyl-amino}-piperidin-1- carbonsäureethyl ester(999) 4 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 1.70E-07 n.d. pyrazol-4-ylmethyl] methylamino} piperidine-1-carboxylic acid ethyl ester
(1000) 1-[5-(2-Fluor-phenyl)-1-(4-pyridin-3-yl- 1.70E-07 n.d. phenyl)-1H-pyrazol-4-ylmethylj-4-methyl- piperazin(1000) 1- [5- (2-fluorophenyl) -1- (4-pyridin-3-yl-1.70E-07 and phenyl) -1H-pyrazol-4-ylmethylj-4-methyl- piperazine
(1001) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1.70E-07 n.d. pyrazol-4-ylmethyl]-(3-imidazol-1-yl-propyl)- amin(1001) [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1.70E-07 n.d. pyrazol-4-ylmethyl] - (3-imidazol-1-yl-propyl) amine
(1002) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1.70E-07 n.d. pyrazol-4-ylmethyl]-[2-(1H-imidazol-4-yl)- ethyl]-amin(1002) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1.70E-07 n.d. pyrazol-4-ylmethyl] - [2- (1H-imidazol-4-yl) ethyl] amine
(1003) 1-[5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 1.70E-07 1.00E-06 1 H-pyrazol-4-ylmethyl]-pyrrolidin-3-ol(1003) 1- [5- (4-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 1.70E-07 1.00E-06 1 H-pyrazol-4-ylmethyl] pyrrolidin-3-ol
(1004) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1 ,80E-07 n.d. pyrazoI-4-ylmethyl]-pyridin-3-ylmethyl-amin(1004) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1, 80E-07 n.d. pyrazol-4-ylmethyl] -pyridine-3-ylmethyl-amine
(1005) [1-(2,,5'-Difluor-biphenyl-4-yl)-5-(2-fluor- 1.80E-07 n.d. phenyl)-1 H-pyrazol-4-ylmethyl]-(1 H-pyrazol-3- yl)-amin(1005) [1- (2, 5'-difluoro-biphenyl-4-yl) -5- (2-fluoro 1.80E-07 nd phenyl) -1 H-pyrazol-4-ylmethyl] - (1 H -pyrazol-3-yl) amine
(1006) N3-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 1 ,80E-07 n.d. pyrazol-4-ylmethyl]-pyridin-3,4-diamin(1006) N3- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-1, 80E-07 n.d. pyrazol-4-ylmethyl] -pyridine-3,4-diamine
(1007) 1-[5-(3,4-Dichlorphenyl)-1-(4'-fluorbiphenyl-4- 1.90E-07 n.d. yl)-1 H-pyrazol-4-ylmethyl]-4-methylpiperazin(1007) 1- [5- (3,4-dichlorophenyl) -1- (4'-fluorobiphenyl-4- 1.90E-07 n.d. yl) -1 H-pyrazol-4-ylmethyl] -4-methylpiperazine
(1008) {1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2.00E-07 n.d. pyrazol-4-ylmethyl]-piperidin-4-yl}-dimethyl- amin(1008) {1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.00E-07 n.d. pyrazol-4-ylmethyl] piperidin-4-yl} dimethyl amine
(1009) 1-(1-Biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4- 2.00E-07 n.d. ylmethyl)-piperazin(1009) 1- (1-biphenyl-4-yl-5-pyridin-2-yl-1 H-pyrazol-4-2.00E-07 n.d. ylmethyl) piperazine
(1010) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyI)-1 H- 2,00E-07 n.d. pyrazol-4-ylmethylj-amino}-N,N-dimethyl- acetamid (1011) 1-Ethyl-4-[1-(4'-fiuorbiphenyl-4-yl)-5-(4- 2.00E-07 n.d. methoxyphenyl)-1H-pyrazol-4-ylmethylj- pipera∑in(1010) 2 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.00E-07 and pyrazol-4-ylmethylj-amino} -N, N-dimethyl-acetamide (1011) 1-Ethyl-4- [1- (4'-fiuorbiphenyl-4-yl) -5- (4- 2.00E-07 and methoxyphenyl) -1H-pyrazol-4-ylmethylj-pipera∑in
(1012) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2,00E-07 n.d. pyrazol-4-ylmethyl]-1H-pyridin-2-on(1012) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.00E-07 n.d. pyrazol-4-ylmethyl] -1H-pyridin-2-one
(1013) 1-[1-(2'-Fluor-biphenyl-4-yl)-5-(4-fluor-phenyl)- 2.10E-07 1 ,00E-06 1 H-pyrazol-4-ylmethyl]-4-methyl-piperazin(1013) 1- [1- (2'-fluoro-biphenyl-4-yl) -5- (4-fluoro-phenyl) - 2.10E-07 1, 00E-06 1 H-pyrazol-4-ylmethyl] - 4-methyl-piperazine
(1014) 3-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.10E-07 n.d. pyrazol-4-ylmethyl]-amino}~ propionsäuremethylester(1014) 3 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.10E-07 n.d. pyrazol-4-ylmethyl] amino} ~ propionic acid methyl ester
(1016) [5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 2.20E-07 1.00E-06 1H-pyrazol-4-ylmethyl]-diethylamin(1016) [5- (4-Chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 2.20E-07 1.00E-06 1H-pyrazol-4-ylmethyl] diethylamine
(1017) 1-[5-(2-Fluor-phenyl)-1-(3'-methyl-biphenyl-4- 2,20E-07 n.d. yl)-1H-pyrazol-4-ylmethyl]-4-methyl-piperazin(1017) 1- [5- (2-fluorophenyl) -1- (3'-methyl-biphenyl-4-2.20E-07nd yl) -1H-pyrazol-4-ylmethyl] -4-methyl- piperazine
(1018) 2-{4-[1-Biphenyl-4-yI-5-(2-fluor-phenyl)-1H- 2.30E-07 n.d. pyrazol-4-ylmethyl]-piperazin-1-yl}-N-ethyl- acetamid(1018) 2- {4- [1-Biphenyl-4-yI-5- (2-fluorophenyl) -1H- 2.30E-07 n.d. pyrazol-4-ylmethyl] -piperazin-1-yl} -N-ethyl-acetamide
(1019) 1-{1-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4- 2.30E-07 4.00E-08 yl)-1 H-pyrazol-4-ylmethyl]-piperidin-4-yl}-1 -(4- fluorphenyl)-methanon (1020) 1-[5-(2-Fluor-phenyl)-1-(2'-methyl-biphenyl-4- 2,30E-07 n.d. yl)-1 H-pyrazol-4-ylmethyl]-4-methyl-piperazin(1019) 1- {1- [5- (2-chlorophenyl) -1- (4'-fluorobiphenyl-4- 2.30E-07 4.00E-08 yl) -1 H-pyrazol-4-ylmethyl] piperidine- 4-yl} -1 - (4-fluorophenyl) methanone (1020) 1- [5- (2-Fluoro-phenyl) -1- (2'-methyl-biphenyl-4- 2.30E-07nd yl) -1 H-pyrazol-4-ylmethyl] -4-methyl piperazine
(1021) 1-[1-(2',5'-Difluor-biphenyl-4-yl)-5-(4-fluor- 2,40E-07 1 ,00E-06 phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyI- piperazin(1021) 1- [1- (2 ', 5'-difluorobiphenyl-4-yl) -5- (4-fluoro-2.40E-07 1, 00E-06 phenyl) -1 H-pyrazole-4 -ylmethyl] -4-methyl-piperazine
(1022) [1-Biphenyl-4-yI-5-(2-fluor-phenyl)-1 H- 2.40E-07 1 ,00E-06 pyra∑oi-4-y Imethyl j-isoxazol-3-y l-am i n(1022) [1-Biphenyl-4-yI-5- (2-fluorophenyl) -1 H- 2.40E-07 1, 00E-06 pyra∑oi-4-y imethyl j-isoxazol-3-y l -am in
(1023) (1-Biphenyl-4-yl-5-phenyl-1 H-pyrazol-4- 2.40E-07 n.d. ylmethyl)-(5-methyl-isoxazoi-3-ylmethyl)-amin(1023) (1-Biphenyl-4-yl-5-phenyl-1H-pyrazol-4- 2.40E-07 n.d. ylmethyl) - (5-methyl-isoxazoi-3-ylmethyl) amine
(1024) N-[5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 2.40E-07 1 ,00E-06 1 H-pyrazol-4-ylmethyl]-N , N', N'-trimethylethan-(1024) N- [5- (4-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 2.40E-07 1, 00E-06 1 H-pyrazol-4-ylmethyl] -N, N ' , N'-trimethylethane
1 ,2-diamin1, 2-diamine
(1025) 1-[1-(4-Bromo-phenyl)-5-phenyl-1 H-pyrazol-4- 2.50E-07 n.d. yl]-4-methyl-piperazin(1025) 1- [1- (4-Bromo-phenyl) -5-phenyl-1 H-pyrazole-4- 2.50E-07 n.d. yl] -4-methyl-piperazine
(1026) 1-(Biphenyl-4-yl-trifluormethyl-1 H-pyrazol-4- 2.60E-07 1.00E-06 ylmethyl)-4-methyl-piperazin(1026) 1- (Biphenyl-4-yl-trifluoromethyl-1 H-pyrazol-4-2.60E-07 1.00E-06 ylmethyl) -4-methyl-piperazine
(1027) 1-[5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 2.60E-07 1 ,00E-06 1 H-pyrazol-4-ylmethyl]-4-cyclopentylpiperazin(1027) 1- [5- (2-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 2.60E-07 1, 00E-06 1 H-pyrazol-4-ylmethyl] -4-cyclopentylpiperazine
(1028) {1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2.70E-07 n.d. pyrazol-4-ylmethyl]-piperidin-2-ylmethyl}- diethyl-amin(1028) {1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.70E-07 n.d. pyrazol-4-ylmethyl] piperidin-2-ylmethyl} diethylamine
(1029) 1-[5-(2-Fluor-phenyl)-1-(4-trifluormethoxy- 2J0E-07 4.90E-07 phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(1029) 1- [5- (2-Fluorophenyl) -1- (4-trifluoromethoxy-2J0E-07 4.90E-07 phenyl) -1 H-pyrazol-4-ylmethyl] -4-methylpiperazine
(1030) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2.70E-07 n.d. pyrazol-4-ylmethyl]-piperidin-4- carbonsäure(2-hydroxy-ethyl)-amid (1031) 2-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.80E-07 n.d. pyrazol-4-ylmethyI]-1 ,3,4,6,7,11b-hexahydro- 2H-pyra∑ino[2,1-a]isochinolin(1030) 1- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.70E-07 and pyrazol-4-ylmethyl] piperidine-4-carboxylic acid (2-hydroxy-ethyl) amide (1031) 2- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1 H-2.80E-07 and pyrazol-4-ylmethyl] -1, 3,4,6,7,11b -hexahydro- 2H-pyra∑ino [2,1-a] isoquinoline
(1032) 2-{4-[1-BiphenyI-4-yl-5-(2-fluor-phenyl)-1 H- 2.80E-07 n.d. pyrazol-4-ylmethyl]-piperazin-1-yl}-ethanol(1032) 2- {4- [1-BiphenyI-4-yl-5- (2-fluorophenyl) -1 H- 2.80E-07 n.d. pyrazol-4-ylmethyl] -piperazin-1-yl} -ethanol
(1033) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 2.80E-07 n.d. pyrazol-4-ylmethyl]-4-ethyl-piperidin-4-ol(1033) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 2.80E-07 n.d. pyrazol-4-yl-methyl] -4-ethyl-piperidin-4-ol
(1034) {[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 2.80E-07 n.d. pyrazol-4-ylmethyl]-amino}-acetonitril(1034) {[1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 2.80E-07 n.d. pyrazol-4-ylmethyl] -amino} -acetonitrile
(1035) 1-(1-Biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4- 2,90E-07 1 ,00E-06 ylmethyl)-4-methyl-piperazin(1035) 1- (1-biphenyl-4-yl-5-pyridin-3-yl-1 H-pyrazol-4- 2.90E-07 1, 00E-06 ylmethyl) -4-methyl-piperazine
(1036) (1-Benzyl-pyrrolidin-3-yl)-[1-biphenyl-4-yl-5- 3,10E-07 n.d. (2-fluor-phenyl)-1H-pyrazol-4-ylmethyl]-amin(1036) (1-Benzyl-pyrrolidin-3-yl) - [1-biphenyl-4-yl-5- 3,10E-07 n.d. (2-fluoro-phenyl) -1H-pyrazol-4-ylmethyl] -amine
(1037) 1-[5-(4-Chlorphenyl)-1-(4*-fluorbiphenyl-4-yl)- 3.10E-07 1.00E-06 1 H-pyrazol-4-ylmethyl]-4-ethylpiperazin(1037) 1- [5- (4-chlorophenyl) -1- (4 * -fluorobiphenyl-4-yl) -3.10E-07 1.00E-06 1 H-pyrazol-4-ylmethyl] -4-ethylpiperazine
(1038) 2-{4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 3.11E-07 n.d. pyrazol-4-ylmethyl]-piperazin-1 -yl}-1 - pyrrolidin-1 -yl-ethanon(1038) 2- {4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-3.11E-07 n.d. pyrazol-4-ylmethyl] piperazin-1-yl} -1 - pyrrolidin-1-yl-ethanone
(1039) Benzyl-[1-biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3.20E-07 n.d. pyrazol-4-ylmethyl]-ethyl-amin(1039) Benzyl- [1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.20E-07 n.d. pyrazol-4-ylmethyl] -ethyl-amine
(1040) 1-[1-(4'-Fluorbiphenyl-4-yl)-5-(4- 3.20E-07 n.d. methoxyphenyl)-1 H-pyrazol-4-ylmethyl]-4- isopropylpipera∑in(1040) 1- [1- (4'-Fluorobiphenyl-4-yl) -5- (4- 3.20E-07 methoxyphenyl) -1 H-pyrazol-4-ylmethyl] -4- isopropylpipera∑in
(1041) (3-A∑a-bicyclo[3.1.0]hex-6-yl)-[1-biphenyl-4- 3.20E-07 n.d. yl-5-(2-fluor-phenyl)-1H-pyrazol-4-ylmethyl]- amm(1041) (3-A∑a-bicyclo [3.1.0] hex-6-yl) - [1-biphenyl-4- 3.20E-07 and yl-5- (2-fluorophenyl) -1H-pyrazole -4-ylmethyl] - amm
(1042) 2-{4-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 3.60E-07 n.d. pyra∑ol-4-ylmethyl]-pipβra∑in-1-yl}-acetarnid(1042) 2- {4- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 3.60E-07 n.d. pyraΣol-4-ylmethyl] -pipβraΣin-1-yl} -acetarnid
(1043) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3.60E-07 n.d. pyrazol-4-yl]-1-morpholin-4-yl-methanon(1043) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.60E-07 n.d. pyrazol-4-yl] -1-morpholin-4-yl-methanone
(1044) [1-(2',5,-Difluor-biphenyl-4-yl)-5-(2-fluor- 3.70E-07 n.d. phenyl)-1 H-pyrazol-4-ylmethyl]-(tetrahydro- furan-2-ylmethyl)-amin(1044) [1- (2 ', 5 , -Difluorobiphenyl-4-yl) -5- (2-fluoro-3.70E-07 and phenyl) -1 H-pyrazol-4-ylmethyl] - (tetrahydro- furan-2-ylmethyl) -amine
(1045) 2-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3.70E-07 n.d. pyrazol-4-ylmethyl]-amino}-3-(3H-imidazol-4- yl)-propan-1-ol(1045) 2 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.70E-07 n.d. pyrazol-4-ylmethyl] amino} -3- (3H-imidazol-4-yl) propan-1-ol
(1046) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3.70E-07 n.d. pyrazol-4-ylmethyl]-(5-methyl-thiazol-2-yl)- amin(1046) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.70E-07 n.d. pyrazol-4-ylmethyl] - (5-methylthiazol-2-yl) amine
(1047) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 3.80E-07 n.d. pyrazol-4-ylmethyl]-4-thiophen-3-ylmethyl- piperazin(1047) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 3.80E-07 n.d. pyrazol-4-ylmethyl] -4-thiophene-3-ylmethylpiperazine
(1048) [5-(2-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 3.80E-07 n.d.(1048) [5- (2-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 3.80E-07 n.d.
1 H-pyrazol-4-yl]-methanol1 H-pyrazol-4-yl] methanol
(1049) 1-[1-(4'-Chlor-biphenyl-3-yl)-5-(2-fluor- 3.90E-07 n.d. phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(1049) 1- [1- (4'-chloro-biphenyl-3-yl) -5- (2-fluoro-3.90E-07 and phenyl) -1 H-pyrazol-4-ylmethyl] -4-methyl- piperazine
(1050) 1-[5-(2-Fluor-phenyl)-1-(5-trifluormethyl- 3.90E-07 n.d. pyridin-2-yl)-1 H-pyrazol-4-ylmethyl]-pyrrolidin-(1050) 1- [5- (2-fluorophenyl) -1- (5-trifluoromethyl-3.90E-07 n.d. pyridin-2-yl) -1 H-pyrazol-4-ylmethyl] pyrrolidine
3-ol3-ol
(1051) 8-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 4.00E-07 1.00E-06 pyrazol-4-ylmethyl]-1 -phenyl- 1 ,3,8-triaza- spiro[4.5]decan-4-on(1051) 8- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 4.00E-07 1.00E-06 pyrazol-4-ylmethyl] -1-phenyl-1, 3,8-triaza-spiro [4.5] decan-4-one
(1052) 1-[5-(3,5-Dichlorphenyl)-1-(4'-fluorbiphenyl-4- 4,OOE-07 n.d. yl)-1 H-pyra∑ol-4-ylmethyl]-4-methylpiperazin(1052) 1- [5- (3,5-dichlorophenyl) -1- (4'-fluorobiphenyl-4- 4, OOE-07 n.d. yl) -1 H-pyra∑ol-4-ylmethyl] -4-methylpiperazine
(1053) 1-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 4.30E-07 n.d. pyrazol-4-ylmethyl]-piperidin-4-oI(1053) 1- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1H- 4.30E-07 n.d. pyrazol-4-ylmethyl] -piperidin-4-oI
(1054) 1-[5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 4.40E-07 1 ,OOE-06(1054) 1- [5- (4-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 4.40E-07 1, OOE-06
1 H-pyrazol-4-ylmethyI]-4-isopropylpiperazin1 H-pyrazol-4-ylmethyl] -4-isopropylpiperazine
(1055) 1-[5-(2-Methoxy-phenyl)-1-(4-thiophen-3-yl- 4.60E-07 3.00E-07 phenyl)-1 H-pyrazol-4-ylmethyl]-4-methyl- piperazin(1055) 1- [5- (2-methoxyphenyl) -1- (4-thiophene-3-yl- 4.60E-07 3.00E-07 phenyl) -1 H-pyrazol-4-ylmethyl] -4- methyl piperazine
(1056) 3-{[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1H- 4.60E-07 n.d. pyrazol-4-ylmethyl]-amino}-pyrrolidin-1- carbonsäuretert-butyl ester(1056) 3 - {[1-biphenyl-4-yl-5- (2-fluorophenyl) -1H- 4.60E-07 n.d. pyrazol-4-ylmethyl] amino} pyrrolidine-1-carboxylic acid tert-butyl ester
(1057) 1-[5-(4-Chlorphenyl)-1-(4'-fluorbiphenyl-4-yl)- 4.60E-07 1.00E-06 1 H-pyrazol-4-ylmethyl]-4-methylpiperazin(1057) 1- [5- (4-chlorophenyl) -1- (4'-fluorobiphenyl-4-yl) - 4.60E-07 1.00E-06 1 H-pyrazol-4-ylmethyl] -4-methylpiperazine
(1058) [1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 4.70E-07 n.d. pyrazol-4-ylmethyl]-piperidin-4-yl-amin(1058) [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H- 4.70E-07 n.d. pyrazol-4-ylmethyl] -piperidin-4-yl-amine
(1059) 2-[1-Biphenyl-4-yl-5-(2-fluor-phenyl)-1 H- 4,70E-07 n.d. pyrazol-4-yl]-ethanol Die nachfolgenden Beispiele betreffen pharmazeutische Zubereitungen:(1059) 2- [1-Biphenyl-4-yl-5- (2-fluorophenyl) -1 H-4.70E-07 and pyrazol-4-yl] ethanol The following examples relate to pharmaceutical preparations:
Beispiel A: InjektionsgläserExample A: Injection glasses
Eine Lösung von 100 g eines Wirkstoffes der Formel I und 5 g Dinatrium- hydrogenphosphat wird in 3 I zweifach destilliertem Wasser mit 2 n Salzsäure auf pH 6,5 eingestellt, steril filtriert, in Injektionsgläser abgefüllt, unter sterilen Bedingungen lyophilisiert und steril verschlossen. Jedes In- jektionsglas enthält 5 mg Wirkstoff.A solution of 100 g of an active ingredient of the formula I and 5 g of disodium hydrogenphosphate is adjusted to pH 6.5 in 3 l of double-distilled water with 2N hydrochloric acid, sterile filtered, filled into injection glasses, lyophilized under sterile conditions and sealed sterile. Each injection glass contains 5 mg of active ingredient.
Beispiel B: SuppositorienExample B: Suppositories
Man schmilzt ein Gemisch von 20 g eines Wirkstoffes der Formel I mit 100 g Sojalecithin und 1400 g Kakaobutter, gießt in Formen und läßt erkalten. Jedes Suppositorium enthält 20 mg Wirkstoff. Beispiel C: LösungA mixture of 20 g of an active ingredient of the formula I is melted with 100 g of soy lecithin and 1400 g of cocoa butter, poured into molds and allowed to cool. Each suppository contains 20 mg of active ingredient. Example C: solution
Man bereitet eine Lösung aus 1 g eines Wirkstoffes der Formel I, 9,38 g NaH2PO4 . 2 H2O, 28,48 g Na2HPO4 . 12 H2O und 0,1 g Benzalkonium- chlorid in 940 ml zweifach destilliertem Wasser. Man stellt auf pH 6,8 ein, füllt auf 1 I auf und sterilisiert durch Bestrahlung. Diese Lösung kann in Form von Augentropfen verwendet werden.A solution is prepared from 1 g of an active ingredient of the formula I, 9.38 g of NaH 2 PO 4 . 2 H 2 O, 28.48 g Na 2 HPO 4 . 12 H 2 O and 0.1 g benzalkonium chloride in 940 ml double-distilled water. It is adjusted to pH 6.8, made up to 1 l and sterilized by irradiation. This solution can be used in the form of eye drops.
Beispiel D: SalbeExample D: ointment
Man mischt 500 mg eines Wirkstoffes der Formel I mit 99,5 g Vaseline unter aseptischen Bedingungen.500 mg of an active ingredient of the formula I are mixed with 99.5 g of petroleum jelly under aseptic conditions.
Beispiel E: TablettenExample E: tablets
Ein Gemisch von 1 kg Wirkstoff der Formel I, 4 kg Lactose, 1 ,2 kg Kartoffelstärke, 0,2 kg Talk und 0,1 kg Magnesiumstearat wird in üblicher Weise zu Tabletten verpreßt, derart, daß jede Tablette 10 mg Wirkstoff enthält. Beispiel F: DrageesA mixture of 1 kg of active ingredient of the formula I, 4 kg of lactose, 1, 2 kg of potato starch, 0.2 kg of talc and 0.1 kg of magnesium stearate is compressed into tablets in a conventional manner such that each tablet contains 10 mg of active ingredient. Example F: coated tablets
Analog Beispiel E werden Tabletten gepreßt, die anschließend in üblicher Weise mit einem Überzug aus Saccharose, Kartoffelstärke, Talk, Tragant und Farbstoff überzogen werden.Analogously to Example E, tablets are pressed, which are then coated in a conventional manner with a coating of sucrose, potato starch, talc, tragacanth and colorant.
Beispiel G: KapselnExample G: capsules
2 kg Wirkstoff der Formel I werden in üblicher Weise in Hartgelatine- kapseln gefüllt, so daß jede Kapsel 20 mg des Wirkstoffs enthält.2 kg of active ingredient of the formula I are filled into hard gelatin capsules in a conventional manner, so that each capsule contains 20 mg of the active ingredient.
Beispiel H: AmpullenExample H: ampoules
Eine Lösung von 1 kg Wirkstoff der Formel I in 60 I zweifach destilliertem Wasser wird steril filtriert, in Ampullen abgefüllt, unter sterilen Bedingungen lyophilisiert und steril verschlossen. Jede Ampulle enthält 10 mg Wirkstoff.A solution of 1 kg of active ingredient of the formula I in 60 l of double-distilled water is sterile filtered, filled into ampoules, lyophilized under sterile conditions and sealed sterile. Each ampoule contains 10 mg of active ingredient.
Beispiel I: Inhalations-SprayExample I: Inhalation Spray
Man löst 14 g Wirkstoff der Formel I in 10 I isotonischer NaCI-Lösung und füllt die Lösung in handelsübliche Sprühgefäße mit Pump-Mechanismus. Die Lösung kann in Mund oder Nase gesprüht werden. Ein Sprühstoß (etwa 0,1 ml) entspricht einer Dosis von etwa 0,14 mg. 14 g of active ingredient of the formula I are dissolved in 10 I of isotonic NaCl solution and the solution is filled into commercially available spray vessels with a pump mechanism. The solution can be sprayed into the mouth or nose. One spray (approximately 0.1 ml) corresponds to a dose of approximately 0.14 mg.

Claims

Patentansprüche claims
1. Verwendung der Verbindungen der Formel1. Use of the compounds of the formula
worin wherein
X CH oder N,X CH or N,
R1 H, A, Hai, (CH2)nHet, (CH2)nAr, Cycloalkyl mit 3 bis 7 C-R 1 H, A, shark, (CH 2 ) n Het, (CH 2 ) n Ar, cycloalkyl with 3 to 7 C-
Atomen, CF3, NO2, CN, C(NH)NOH oder OCF3,Atoms, CF 3 , NO 2 , CN, C (NH) NOH or OCF 3 ,
R2 (CH2)nHet, (CH2)πAr, Cycloalkyl mit 3 bis 7 C-Atomen oder CF3,R 2 (CH 2 ) n Het, (CH 2 ) π Ar, cycloalkyl with 3 to 7 C atoms or CF 3 ,
R3, R4 H, (CH2)nCO2R5, (CH2)nCOHet, (CH2)nCON(R5)2,R 3 , R 4 H, (CH 2 ) n CO 2 R 5 , (CH 2 ) n COHet, (CH 2 ) n CON (R 5 ) 2 ,
(CH2)nCOO(CH2)nHet, CHO, (CH2)nOR5, (CH2)nHet, (CH2)nN(R5)2, CH=N-OA, CH2CH=N-OA, (CH2)nNHOA, (CH2)nN(R5)Het, (CH2)nCH=N-Het, (CH2)nOCOR5, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2CH2OCF3, (CH2)nN(R5)C(R5)HCOOR5, (CH2)nN(R5)CH2COHet, (CH2)nN(R5)CH2Het, (CH2)nN(R5)CH2CH2Het, (CH2)nN(R5)CH2CH2N(R5)CH2COOR5, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2CH2N(R5)2, CH=CHCOOR5, CH=CHCH2NR6Het, CH=CHCH2N(R5)2, CH=CHCH2OR5, CH=CHCH2Het, (CH2)nN(R5)Ar, (CH2)nN(COOR5)COOR5, (CH2)nN(CONH2)COOR5, (CH2)nN(CONH2)CONH2, (CH2)nN(CH2COOR5)COOR5, (CH2)nN(CH2CONH2)COOR5, (CH2)nN(CH2CONH2)CONH2, (CH2)nCHR5COR5, (CH2)nCHR5COOR5, (CH2)nCHR5CH2OR5, wobei jeweils einer der Reste R3 oder R4 die Bedeutung H aufweist, R5 H oderA(CH 2 ) n COO (CH 2 ) n Het, CHO, (CH 2 ) n OR 5 , (CH 2 ) n Het, (CH 2 ) n N (R 5 ) 2 , CH = N-OA, CH 2 CH = N-OA, (CH 2 ) n NHOA, (CH 2 ) n N (R 5 ) Het, (CH 2 ) n CH = N-Het, (CH 2 ) n OCOR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) nN (R 5 ) CH 2 CH 2 OCF 3 , (CH 2 ) n N (R 5 ) C (R 5 ) HCOOR 5 , (CH 2 ) n N (R 5 ) CH 2 COHet, (CH 2 ) n N (R 5 ) CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) CH 2 COOR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) 2 , CH = CHCOOR 5 , CH = CHCH 2 NR 6 Het, CH = CHCH 2 N (R 5 ) 2 , CH = CHCH 2 OR 5 , CH = CHCH 2 Het, (CH 2 ) n N (R 5 ) Ar, (CH 2 ) n N (COOR 5 ) COOR 5 , (CH 2 ) n N (CONH 2 ) COOR 5 , (CH 2 ) n N (CONH 2 ) CONH 2 , (CH 2 ) n N (CH 2 COOR 5 ) COOR 5 , (CH 2 ) n N (CH 2 CONH 2 ) COOR 5 , (CH 2 ) n N (CH 2 CONH 2 ) CONH 2 , (CH 2 ) n CHR 5 COR 5 , (CH 2 ) n CHR 5 COOR 5 , (CH 2 ) n CHR 5 CH 2 OR 5 , where in each case one of the radicals R 3 or R 4 has the meaning H, R 5 H or A
A unsubstituiertes oder durch Hai oder CN substituiertes geradkettiges oder verzweigtes Alkyl oder Cycloalkyl mit 2 bis 4 C-Atomen, mit 1 bis 10 C-Atomen, Alkenyl mit 2 bis 10 G-A unsubstituted or substituted by shark or CN straight-chain or branched alkyl or cycloalkyl with 2 to 4 carbon atoms, with 1 to 10 carbon atoms, alkenyl with 2 to 10 carbon atoms
Atomen, Alkoxyalkyl mit 2 bis 10 C-Atomen oder Cycloalkyl mit 4 bis 7 C-Atomen,Atoms, alkoxyalkyl with 2 to 10 C atoms or cycloalkyl with 4 to 7 C atoms,
Het bevorzugt einen unsubstituierten oder einfach oder mehrfach 0 durch A und/oder Hai substituierten, gesättigten, ungesättigten oder aromatischen mono- oder bicyclischen heterocyclischen oder einen ein oder zwei Heteroatome enthaltenden linearen Rest mit 1 bis 15 C-Atomen,Het preferably an unsubstituted or mono- or polysubstituted O by A and / or shark, saturated, unsaturated or aromatic mono- or bicyclic heterocyclic or a linear radical containing one or two heteroatoms and having 1 to 15 carbon atoms,
5 Ar einen unsubstituierten oder einfach oder mehrfach durch A und/oder Hai, OR5, OOCR5, COOR5, CON(R5)2, CN, NO2, NH2, NHCOR5, CF3 oder SO2CH3 substituierten Phenylrest,5 Ar is an unsubstituted or mono- or polysubstituted by A and / or shark, OR 5 , OOCR 5 , COOR 5 , CON (R 5 ) 2 , CN, NO 2 , NH 2 , NHCOR 5 , CF 3 or SO 2 CH 3 phenyl,
n 0, 1 , 2, 3, 4 oder 5 0 undn 0, 1, 2, 3, 4 or 5 0 and
Hai F, Cl, Br oder lShark F, Cl, Br or l
5 bedeuten, sowie deren Salze und Solvate, Enantiomere und5 mean, and their salts and solvates, enantiomers and
Racemate, zur Herstellung eines Arzneimittels zur Behandlung und Prophylaxe von Krankheiten, die durch die Bindung der Verbindungen der Formel I an 5 HT-Rezeptoren beeinflusst werden können. 0Racemate, for the manufacture of a medicament for the treatment and prophylaxis of diseases which can be influenced by the binding of the compounds of the formula I to 5 HT receptors. 0
2. Verwendung von Verbindungen gemäß Anspruch 1 und/oder von deren physiologisch unbedenklichen Salzen und Solvaten zur Herstellung eines Arzneimittels mit 5-HT-Rezeptor-antagonistischer Wirkung. O 2. Use of compounds according to claim 1 and / or of their physiologically acceptable salts and solvates for the manufacture of a medicament with 5-HT receptor antagonistic effect. O
3. Verwendung von Verbindungen gemäß Anspruch 1 oder 2 und/oder von deren physiologisch unbedenklichen Salzen und Solvaten zur Herstellung eines Arzneimittels mit 5-HT2A-Rezeptor-antagonistischer Wirkung.3. Use of compounds according to claim 1 or 2 and / or of their physiologically acceptable salts and solvates for the manufacture of a medicament with 5-HT 2A receptor antagonistic effect.
4. Verwendung von Verbindungen der Formel I nach Anspruch 1, 2 oder 3 und/oder ihre physiologisch unbedenklichen Salze oder Solvate zur Herstellung eines Arzneimittels zur Prophylaxe und/oder Behandlung von Psychosen, neurologischen Störungen, amyotropher Lateral- Sklerose, Essstörungen wie Bulimie, nervöser Anorexie, des prämenstrualen Syndroms und/oder zur positiven Beeinflussung von Zwangsverhalten (obsessive-compulsive disorder, OCD).4. Use of compounds of formula I according to claim 1, 2 or 3 and / or their physiologically acceptable salts or solvates for the manufacture of a medicament for the prophylaxis and / or treatment of psychoses, neurological disorders, amyotrophic lateral sclerosis, eating disorders such as bulimia, nervous Anorexia, premenstrual syndrome and / or to positively influence compulsive behavior (obsessive-compulsive disorder, OCD).
5. Verwendung der Verbindungen der Formel I nach einem oder mehreren der vorhergehenden Ansprüche, worin R Phenyl, 2-, 3- oder 4-Cyanophenyl, 2-, 3- oder 4-Fluorphenyl, 2-, 3- oder 4-Methyl-, Ethyl-, n-Propyl- oder n-Butyiphenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5- oder 3,6-Difluor- , Dichlor- oder Dicyanophenyl, 3,4,5-Trifluorphenyl, 3,4,5-Trimethoxy- oder Triethoxyphenyl, Thiophen-2-yl oder Thiophen-3-yl oder 1-, 2- oder 3-Pyrrolyl bedeutet.5. Use of the compounds of formula I according to one or more of the preceding claims, wherein R is phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl- , Ethyl, n-propyl or n-butyiphenyl, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, 3,5- or 3,6-difluoro-, Dichloro- or dicyanophenyl, 3,4,5-trifluorophenyl, 3,4,5-trimethoxy- or triethoxyphenyl, thiophene-2-yl or thiophene-3-yl or 1-, 2- or 3-pyrrolyl.
6. Verwendung der Verbindungen der Formel I nach einem oder mehreren der vorhergehenden Ansprüche, worin R3 (CH2)nCO2R5, (CH2)nCO-Het, CHO, CH2OR5, (CH2)n-Het, (CH2)nN(R5)2 oder CH=N- OA, (CH2)nN(R5)Het, (CH2)nN(R5)CH2CH2OR5, (CH2)nN(R5)CH2Het,6. Use of the compounds of formula I according to one or more of the preceding claims, wherein R 3 (CH 2 ) n CO 2 R 5 , (CH 2 ) n CO-Het, CHO, CH 2 OR 5 , (CH 2 ) n -Het, (CH 2 ) n N (R 5 ) 2 or CH = N- OA, (CH 2 ) n N (R 5 ) Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 OR 5 , (CH 2 ) n N (R 5 ) CH 2 Het,
(CH2)nN(R5)CH2CH2Het, (CH2)nN(R5)CH2CH2N(R5)2, CH=CHCH2NR5Het, CH=CHCH2N(R5)2, CH=CHCH2OR5, CH=CHCH2Het oder (CH2)nN(R5)Ar bedeutet.(CH 2 ) n N (R 5 ) CH 2 CH 2 Het, (CH 2 ) n N (R 5 ) CH 2 CH 2 N (R 5 ) 2 , CH = CHCH 2 NR 5 Het, CH = CHCH 2 N (R 5 ) 2 , CH = CHCH 2 OR 5 , CH = CHCH 2 Het or (CH 2 ) n N (R 5 ) Ar.
7. Verwendung der Verbindungen der Formel I nach einem oder mehreren der vorhergehenden Ansprüche, worin R4 H bedeutet.7. Use of the compounds of formula I according to one or more of the preceding claims, wherein R 4 is H.
8. Verwendung der Verbindungen der Formel I nach einem oder mehreren der vorhergehenden Ansprüche, worin R2 Phenyl, 2-, 3- oder 4-Cyanophenyl, 2-, 3- oder 4-Fluorphenyl, 2-, 3- oder 4-Methyl-,8. Use of the compounds of formula I according to one or more of the preceding claims, wherein R 2 is phenyl, 2-, 3- or 4-cyanophenyl, 2-, 3- or 4-fluorophenyl, 2-, 3- or 4-methyl -
Ethyl-, n-Propyl- oder n-Butylphenyl, 2,3-, 2,4-, 2,5-, 2,6-Difluor- oder Dicyanophenyl, Thiophen-2-yI oder Thiophen-3-yl, 2-, 3- oder 4- Pyridyl, 2-, 4- oder 5-Oxazolyl, 2-, 4- oder 5-Thiazolyl, Chinolinyl, Isochinolinyl, 2- oder 4-Pyridazyl, 2-, 4- oder 5-Pyrimidyl, 2- oder 3- Pyra∑inyl, 2- oder 3-Furyl bedeutet.Ethyl, n-propyl or n-butylphenyl, 2,3-, 2,4-, 2,5-, 2,6-difluoro or Dicyanophenyl, thiophene-2-yl or thiophene-3-yl, 2-, 3- or 4-pyridyl, 2-, 4- or 5-oxazolyl, 2-, 4- or 5-thiazolyl, quinolinyl, isoquinolinyl, 2- or 4-pyridazyl, 2-, 4- or 5-pyrimidyl, 2- or 3-pyra∑inyl, 2- or 3-furyl.
9. Verwendung der Verbindungen der Formel I nach einem oder mehreren der vorhergehenden Ansprüche, worin X die Bedeutung CH aufweist.9. Use of the compounds of formula I according to one or more of the preceding claims, wherein X has the meaning CH.
10. Verwendung der Verbindungen der Formel (a) bis (o) gemäß10. Use of the compounds of formula (a) to (o) according to
Anspruch 1:Claim 1:
[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-ylmethyl]- (a)[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] - (a)
(4-methyl-piperazin-1 -yl)-amin(4-methyl-piperazin-1-yl) amine
4-{2-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl]- (b) ethylj-morpholin4- {2- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl] - (b) ethylj-morpholine
4-{3-[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-yl]- (c) allylj-morpholin4- {3- [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-yl] - (c) allylj-morpholine
1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (d) ylmethyl]-pyrrolidin-3-ol1- [1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (d) ylmethyl] pyrrolidin-3-ol
1 -[1 -(4'-Fluoro-biphenyl-4-yl)-5-(2-f luoro-phenyl)-1 H- (e) pyrazol-4-ylmethyl]-4-methyl-piperazin1 - [1 - (4'-Fluoro-biphenyl-4-yl) -5- (2-f luoro-phenyl) -1 H- (e) pyrazol-4-ylmethyl] -4-methyl-piperazine
1 -[5-(2-Fluoro-phenyl)-1 -(4-thiophen-3-yl-phenyl)-1 H- (f) pyrazol-4-ylmethyl]-4-methyl-piperazin1 - [5- (2-Fluoro-phenyl) -1 - (4-thiophene-3-yl-phenyl) -1 H- (f) pyrazol-4-ylmethyl] -4-methyl-piperazine
1-[5-Furan-2-yl-1-(4-thiophen-3-yl-phenyl)-1 H-pyrazol-4- (g) ylmethyl]-4-methyl-piperazin1- [5-Furan-2-yl-1- (4-thiophene-3-yl-phenyl) -1 H-pyrazol-4- (g) ylmethyl] -4-methyl-piperazine
N1-[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (h) ylmethyl]-ethan-1 ,2-diamin 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (i) ylmethyl]-amino}-ethanolN 1 - [1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H -pyrazol-4- (h) ylmethyl] -ethan-1,2-diamine 2 - {[1-biphenyl- 4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (i) ylmethyl] amino} ethanol
[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-ylmethyl]- (j)[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] - (j)
(2-methoxy-ethyl)-amin 2-{[1-Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (k) ylmethylj-methyl-amino}-ethanol 1 -[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4- (I) ylmethyl]-4-methyl-[1,4]diazepam(2-methoxyethyl) amine 2 - {[1-biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (k) ylmethylj-methylamino} ethanol 1 - [1 -Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4- (I) ylmethyl] -4-methyl- [1,4] diazepam
1 -[1 -(4'-Fluoro-biphenyl-4-yl)-5-phenyl-1 H-pyrazol-4- (m) ylmethyl]-4-methyl-piperazin 1-[5-(2-FIuoro-phenyl)-1-(4-pyrrol-1-yl-phenyl)-1 H-pyrazol- (n)1 - [1 - (4'-Fluoro-biphenyl-4-yl) -5-phenyl-1 H-pyrazol-4- (m) ylmethyl] -4-methyl-piperazine 1- [5- (2-fluorine phenyl) -1- (4-pyrrol-1-yl-phenyl) -1 H-pyrazole- (n)
4-ylmethyl]-4-methyl-piperazin4-ylmethyl] -4-methyl-piperazine
[1 -Biphenyl-4-yl-5-(2-fluoro-phenyl)-1 H-pyrazol-4-ylmethyI]- (o) methyl-(1-methyl-pyrrolidin-3-yl)-amin[1-Biphenyl-4-yl-5- (2-fluoro-phenyl) -1 H-pyrazol-4-ylmethyl] - (o) methyl- (1-methyl-pyrrolidin-3-yl) amine
sowie deren Salze und Solvate. and their salts and solvates.
EP04718277A 2003-04-05 2004-03-08 Substituted pyrazoles Withdrawn EP1626967A1 (en)

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