HRP20192336T1 - Derivati imidazotiadiazola i imidazopirazina kao inhibitori proteazom aktiviranog receptora 4 (par4) za liječenje agregacije trombocita - Google Patents
Derivati imidazotiadiazola i imidazopirazina kao inhibitori proteazom aktiviranog receptora 4 (par4) za liječenje agregacije trombocita Download PDFInfo
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- HRP20192336T1 HRP20192336T1 HRP20192336TT HRP20192336T HRP20192336T1 HR P20192336 T1 HRP20192336 T1 HR P20192336T1 HR P20192336T T HRP20192336T T HR P20192336TT HR P20192336 T HRP20192336 T HR P20192336T HR P20192336 T1 HRP20192336 T1 HR P20192336T1
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- BOXRDDIXJOUZLV-UHFFFAOYSA-N 2h-imidazo[4,5-d]thiadiazole Chemical compound N1SC2=NC=NC2=N1 BOXRDDIXJOUZLV-UHFFFAOYSA-N 0.000 title 1
- 102100040853 PRKC apoptosis WT1 regulator protein Human genes 0.000 title 1
- 101710162991 PRKC apoptosis WT1 regulator protein Proteins 0.000 title 1
- 102000004885 Protease-activated receptor 4 Human genes 0.000 title 1
- 108090001010 Protease-activated receptor 4 Proteins 0.000 title 1
- 150000005235 imidazopyrazines Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 claims 45
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 30
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 22
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 21
- -1 halo-C1-C4 alkoxy Chemical group 0.000 claims 21
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 21
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 21
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 15
- 230000009424 thromboembolic effect Effects 0.000 claims 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 101100243950 Arabidopsis thaliana PIE1 gene Proteins 0.000 claims 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims 12
- 125000001153 fluoro group Chemical group F* 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 229910052736 halogen Inorganic materials 0.000 claims 7
- 150000002367 halogens Chemical class 0.000 claims 7
- 125000005842 heteroatom Chemical group 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 229910052801 chlorine Inorganic materials 0.000 claims 6
- 239000000460 chlorine Substances 0.000 claims 6
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- 229910052717 sulfur Inorganic materials 0.000 claims 6
- 125000004414 alkyl thio group Chemical group 0.000 claims 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims 5
- 125000004043 oxo group Chemical group O=* 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical group F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims 4
- 108010081348 HRT1 protein Hairy Chemical group 0.000 claims 4
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 claims 4
- 230000002526 effect on cardiovascular system Effects 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 3
- 101150020251 NR13 gene Proteins 0.000 claims 3
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 2
- 125000004450 alkenylene group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000005647 linker group Chemical group 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 2
- 230000003836 peripheral circulation Effects 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 238000011321 prophylaxis Methods 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- 150000003852 triazoles Chemical class 0.000 claims 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims 1
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims 1
- 125000005529 alkyleneoxy group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
- A61K31/433—Thidiazoles
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- A—HUMAN NECESSITIES
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/041—Heterocyclic compounds
- A61K51/044—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K51/0453—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
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Claims (15)
1. Spoj sa formulom I:
ili stereoizomer, tautomer, farmaceutski prihvatljiva sol ili solvat istog, gdje:
WjeO;
R0 je R1;
Y je S ili -CR8=CR9-;
R1 je nezavisno odabran od grupe koja se sastoji od:
H,
halo,
C1-C2 alkila,
ciklopropila,
C1-C2 alkoksi,
C1-C2 alkiltio,
halo-C1-C2-alkila, koji sadrži 1 do 5 halogena, gdje je halo F ili Cl, i
halo-C3-C4 cikloalkila;
R8 i R9 su nezavisno odabrani od grupe koja se sastoji od:
H,
fluoro,
kloro,
C1-C3 alkila,
C1-C2 alkoksi, i
halo-C1-C2 alkila;
pod uvjetom da najmanje jedan od R1, R8 i R9 je drugačije od H;
R2 je H,
X1 je odabran od grupe koja se sastoji od CH ili N;
X2, X3 i X4 su nezavisno odabrani od CR3;
R3 je odabran od grupe koja se sastoji od H, C1-C3 alkila, C1-C3 alkoksi, fluoro, kloro, OCF3, i halo-C1-C2-alkila, koji sadrži 1 do 5 halogena;
R4 i R5 su nezavisno odabrani od H i metila;
je heteroaril prsten sa 5 članova odabran od tiazola, tiadiazola, oksazola, oksadiazola, i triazola;
R6 je odabran od grupe koja se sastoji od H, halo, OCF3, OCHF2, OH, CN, NO2, NR11R12, C1-C4 alkoksikarbonila, (C=O)NR11R12 i C1-C5 alkila koji je supstituiran sa 0 do 7 grupa koje su nezavisno odabrane od halo, CF3, OCF3, OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, C1-C4 alkoksi-C1-C4 alkoksi, di-C1-C4-alkilaminofenil-C1-C4-alkila, (di-C1-C4-alkoksi-C1-C4-alkil)-C1-C4-alkila, di-C1-C4-alkilamino, C3-C6-cikloalkila, i C1-C4 alkiltio, ili
R6 je B-D-, gdje D je veznik, koji je odabran od:
jednostruke veze,
-O-,
-S-,
C1-C4 alkilena koji je supstituiran sa 0 do 4 grupe koje su nezavisno odabrane od halo ili OH,
C1-C4 alkilenoksi,
C2-C6 alkenilena, i
B je odabran iz grupe koja se sastoji od:
C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i 5-6-očlanog heteroarila,
5- do 10-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, 5-6-očlanog heteroarila, i (CH2)fenila,
4- do 10-očlanog heterociklila koji sadrži atome ugljika i 1 do 2 dodatna heteroatoma odabrana od N, O, i S, i supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, okso, -(CHR13)n1-5- ili 6-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; NR13S(O)R14, NR13SO2R14, -(CHR13)n1-4- do 10-očlanog-heterociklila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, halo-C1-C4 alkoksi, di-C1-C4-alkilamino-C1-C4-alkila, NR11R12, cijano, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, C1-C4-alkoksi-C1-C4-alkila, C3-C6 cikloalkil-C1-C4-alkilkarbonila, C6-C10 arilkarbonila, C1-C4-alkilkarboniloksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, C1-C4-alkoksikarbonila, (C=O)NR11R12, CF3, OCF3, i CF2CH3;
C3-C6 cikloalkila koji može sadržati nezasićenje, supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, C6-C10 arila, COOH, okso, C1-C4-alkoksikarbonila, (C=O)NR11R12, i C1-C4 alkila; i
C5-C11 spirocikloalkila koji može da sadrži nezasićenje i koji po izboru sadrži 1 do 3 heteroatoma odabrana od O, N ili S i supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, hidroksi-C1-C4-alkila, C6-C10 arila, i C1-C4 alkila;
R11 i R12 su nezavisno, pri svakom pojavljivanju, odabrani iz grupe koja se sastoji od:
H,
C1-C4 alkila,
halo-C1-C4-alkila,
C2-C4 alkenila,
-(CR14R14)n1-fenila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, OCHF2, di-C1-C4-alkilamino, i cijano,
-(CHR13)n1-C3-C6-cikloalkila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, hidroksi-C1-C4-alkila, i C1-C4 alkila,
-(CHR13)n1-4- do 10-očlanog-heterociklila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, i C1-C4 alkila,
-(CHR13 )n1-5- do 10-očlanog-heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, hidroksi-C1-C4-alkila, i C1-C4 alkila,
di-C1-C4-alkilamino-C1-C4-alkila,
di-C1-C4-alkoksi-C1-C4-alkila,
hidroksi-C1-C4-alkila,
cijano-C1-C4-alkila,
C1-C4-alkoksi-C1-C4-alkila,
C1-C4-alkoksikarbonil-C1-C4-alkila,
C1-C4-alkoksikarbonila,
C1-C4-alkilkarbonila,
fenilkarbonila;
C1-C4-alkoksikarbonilamino-C1-C4-alkilkarbonila, i
di-C1-C4-alkilamino-C1-C4-alkilkarbonila,
alternativno, R11 i R12, kada su vezani za isti dušik, kombiniraju se da formiraju 4- do 8-očlani heterociklični prsten koji sadrži atome ugljika supstituirane sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, CHF2, OCF3, OCHF2, OCH2F, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, C1-C4 alkila i C1-C4 alkoksi, i 0 do 2 dodatna heteroatoma odabrana od N, NR13, O i S(O)p;
R13 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, C1-C6 alkila i -(CH2)fenila;
R14 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, C1-C6 alkila, halo-C1-C4-alkila, C1-C4-alkoksikarbonilamino i -(CH2)n1fenila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, OCHF2, di-C1-C4-alkilamino, i cijano,
R7 je odabran iz grupe koja se sastoji od H, halo, hidroksila, okso, C1-C3 alkila, hidroksi-C1-C3-alkila, i halo-C1-C2-alkila, koji sadrži 1 do 5 halogena;
n1, pri svakom pojavljivanju, je odabrano od 0, 1, 2 ili 3; i
p, pri svakom pojavljivanju, je odabrano od 0, 1 i 2.
2. Spoj iz patentnog zahtjeva 1, ili stereoizomer, tautomer, farmaceutski prihvatljiva sol ili solvat istog, gdje:
WjeO;
R0 je R1;
Y je S ili -CR8=CR9-;
R1 je nezavisno odabran iz grupe koja se sastoji od:
H,
fluoro,
kloro,
C1-C2 alkila,
C1-C2 alkoksi,
C1-C2 alkiltio, i
halo-C1-C2-alkila, koji sadrži 1 do 5 halogena, gdje halo je F ili Cl;
R8 i R9 su nezavisno odabrani iz grupe koja se sastoji od:
H,
fluoro,
kloro,
CH3,
OCH3,
CF3, i
CHF2;
pod uvjetom da najmanje jedan od R1, R8 i R9 je drugačiji od H;
R2 je H;
X1 je odabran iz grupe koja se sastoji od CH ili N;
X2 i X4 su CH;
X3 je CR3;
R3 je odabran iz grupe koja se sastoji od H, C1-C3 alkila, C1-C3 alkoksi, fluoro, kloro, OCF3, i halo-C1-C2-alkila, koji sadrži 1 do 5 halogena;
R4 i R5 su nezavisno odabrani od H i metila;
je 5-očlani heteroaril prsten odabran od tiazola, tiadiazola, oksazola, oksadiazola, i triazola;
R6 je odabran iz grupe koja se sastoji od H, halo, OCF3, OCHF2, OH, NR11R12, C1-C4 alkoksikarbonila, (C=O)NR11R12 i C1-C5 alkila supstituiranog sa 0 do 7 grupa nezavisno odabranih od halo, CF3, OCF3, OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, C1-C4 alkoksi-C1-C4 alkoksi, di-C1-C4-alkilaminofenil-C1-C4-alkila, (di-C1-C4-alkoksi-C1-C4-alkil)-C1-C4-alkila, di-C1-C4-alkilamino, C3-C6-cikloalkila, i C1-C4 alkiltio, ili
R6 je B-D-, gdje D je veznik, koji je odabran od:
jednostruke veze,
-O-,
-S-,
C1-C4 alkilena supstituiranog sa 0 do 4 grupe nezavisno odabrane od halo ili OH, i
C2-C6 alkenilena, i
B je odabran iz grupe koja se sastoji od:
C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i 5-6-očlanog heteroarila,
5- do 10-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, 5-6-očlanog heteroarila, i (CH2)fenila,
4- do 10-očlanog heterociklila koji sadrži atome ugljika i 1 do 2 dodatna heteroatoma odabrana od N, O, i S, i supstituiranog sa 0 do 3 grupe nezavisno odabrane od grupe koja se sastoji od halo, okso, -(CHR13)n1-5- ili 6-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; NR13S(O)R14, NR13SO2R14, -(CHR13)n1-4- do 10-očlanog-heterociklila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, halo-C1-C4 alkoksi, di-C1-C4-alkilamino-C1-C4-alkila, NR11R12, cijano, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, C1-C4-alkoksi-C1-C4-alkila, C3-C6 cikloalkil-C1-C4-alkilkarbonila, C6-C10 arilkarbonila, C1-C4-alkilkarboniloksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, C1-C4-alkoksikarbonila, (C=O)NR11R12, CF3, OCF3, i CF2CH3; i
C3-C6 cikloalkila koji može da sadrži nezasićenje, supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, C6-C10 arila, COOH, okso, C1-C4-alkoksikarbonila, (C=O)NR11R12, i C1-C4 alkila;
R11 i R12 su nezavisno, pri svakom pojavljivanju, odabrani iz grupe koja se sastoji od:
H,
C1-C4 alkila,
halo-C1-C4-alkila,
C2-C4 alkenila,
-(CR14R14)n1-fenila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, OCHF2, di-C1-C4-alkilamino, i cijano,
-(CHR13)n1-C3-C6-cikloalkila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, hidroksi-C1-C4-alkila, i C1-C4 alkila,
-(CHR13)n1-4- do 10-očlanog-heterociklila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, i C1-C4 alkila,
-(CHR13)n1-5- do 10-očlanog-heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, hidroksi-C1-C4-alkila, i C1-C4 alkila,
di-C1-C4-alkilamino-C1-C4-alkila,
di-C1-C4-alkoksi-C1-C4-alkila,
hidroksi-C1-C4-alkila,
cijano-C1-C4-alkila,
C1-C4-alkoksi-C1-C4-alkila,
C1-C4-alkoksikarbonil-C1-C4-alkila,
C1-C4-alkoksikarbonila,
C1-C4-alkilkarbonila, i
fenilkarbonila;
alternativno, R11 i R12, kada su vezani za isti dušik, kombiniraju se da formiraju 4- do 8-očlani heterociklični prsten koji sadrži atome ugljika supstituirane sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, CHF2, OCF3, OCHF2, OCH2F, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, C1-C4 alkila i C1-C4 alkoksi, i 0 do 2 dodatna heteroatoma odabrana od N, NR13, O i S(O)p;
R13 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, i C1-C3 alkila;
R14 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, C1-C3 alkila, i halo-C1-C2-alkila;
R7 je odabran iz grupe koja se sastoji od H, fluoro, kloro, okso, C1-C3 alkila, hidroksi-C1-C3-alkila, i halo-C1-C2-alkila, koji sadrži 1 do 5 halogena;
n1, pri svakom pojavljivanju, je odabrano od 0, 1, 2 ili 3; i
p, pri svakom pojavljivanju, je odabrano od 0, 1 i 2.
3. Spoj iz patentnog zahtjeva 1, ili stereoizomer, tautomer, farmaceutski prihvatljiva sol ili solvat istog, gdje:
WjeO;
R0 je R1;
Y je S ili -CH=CH-;
R1 je nezavisno odabran iz grupe koja se sastoji od:
kloro,
CH3,
OCH3,
SCH3,
CHFCH3, i
CF2CH3;
R2 je H;
X1 je CH;
X2 i X4 su CH;
X3 je CR3;
R3 je odabran iz grupe koja se sastoji od OCH3, fluoro, i kloro;
R4 i R5 su nezavisno odabrani od H i CH3;
je 5-očlani heteroaril prsten odabran od tiazola i oksazola;
R6 je odabran iz grupe koja se sastoji od, NR11R12, i C1-C5 alkila supstituiranog sa 0 do 3 grupe nezavisno odabrane od halo, CF3, OCF3, OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, C1-C4 alkoksi-C1-C4 alkoksi, di-C1-C4-alkilaminofenil-C1-C4-alkila, (di-C1-C4-alkoksi-C1-C4-alkil)-C1-C4-alkila, di-C1-C4-alkilamino, C3-C6-cikloalkila, i C1-C4 alkiltio, ili
R6 je B-D-, gdje D je jednostruka veza;
B je odabran iz grupe koja se sastoji od:
C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i 5-6-očlanog heteroarila,
5- do 10-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, halo-C1-C4 alkoksi, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, cijano, nitro, NR11R12, OH, C1-C4-alkilkarboniloksi-C1-C4-alkila, hidroksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, NR13S(O)R14, NR13SO2R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, 5-6-očlanog heteroarila, i (CH2)fenila,
4- do 10-očlanog heterociklila koji sadrži atome ugljika i 1 do 2 dodatna heteroatoma odabrana od N, O, i S, i supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, okso, -(CHR13)n1-5- ili 6-očlanog heteroarila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; NR13S(O)R14, NR13SO2R14, -(CHR13)n1-4- do 10-očlanog-heterociklila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, CF3, OCF3, i CF2CH3; OH, hidroksi-C1-C4-alkila, C1-C4 alkoksi, halo-C1-C4 alkoksi, di-C1-C4-alkilamino-C1-C4-alkila, NR11R12, cijano, C1-C4 alkila, halo-C1-C4 alkila, C3-C6 cikloalkila, C1-C4-alkoksi-C1-C4-alkila, C3-C6 cikloalkil-C1-C4-alkilkarbonila, C6-C10 arilkarbonila, C1-C4-alkilkarboniloksi-C1-C4-alkila, COOR14, SO2R14, (C=O)NR11R12, SO2NR11R12, N(R13)(C=O)NR11R12, N(R13)(C=O)OR14, N(R13)(C=O)R14, O(C=O)NR11R12, O(C=O)OR14, O(C=O)R14, (C=O)OR14, i C6-C10 arila supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, C1-C4 alkoksi, C1-C4 alkila, ciklopropila, C1-C4-alkoksikarbonila, (C=O)NR11R12, CF3, OCF3, i CF2CH3; i
C3-C6 cikloalkila koji može da sadrži nezasićenje, supstituiranog sa 0 do 3 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, OCF3, 5- ili 6-očlanog heteroarila, OH, okso, hidroksi-C1-C4-alkila, C6-C10 arila, COOH, okso, C1-C4-alkoksikarbonila, (C=O)NR11R12, i C1-C4 alkila;
R11 i R12 su nezavisno, pri svakom pojavljivanju, odabrani iz grupe koja se sastoji od:
H,
C1-C4 alkila,
halo-C1-C4-alkila,
di-C1-C4-alkilamino-C1-C4-alkila,
di-C1-C4-alkoksi-C1-C4-alkila,
hidroksi-C1-C4-alkila,
cijano-C1-C4-alkila,
C1-C4-alkoksi-C1-C4-alkila,
C1-C4-alkoksikarbonil-C1-C4-alkila, i
C1-C4-alkoksikarbonila;
alternativno, R11 i R12, kada su vezani za isti dušik, kombiniraju se da formiraju 4- do 7-očlani heterociklični prsten koji sadrži atome ugljika supstituirane sa 0 do 2 grupe nezavisno odabrane iz grupe koja se sastoji od halo, CF3, CHF2, OCF3, OCHF2, OCH2F, OH, okso, hidroksi-C1-C2-alkila, C1-C3 alkila i C1-C3 alkoksi, i 0 do 2 dodatna heteroatoma odabrana od N, NR13, O i S(O)p;
R13 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, i C1-C3 alkila;
R14 je nezavisno, pri svakom pojavljivanju, odabran iz grupe koja se sastoji od H, i C1-C3 alkila
R7 je odabran iz grupe koja se sastoji od H, fluoro, kloro, C1-C3 alkila, hidroksi-C1-C3-alkila, i halo-C1-C2-alkila, koji sadrži 1 do 5 halogena;
n1, pri svakom pojavljivanju, je odabrano od 0, 1, 2 ili 3; i
p, pri svakom pojavljivanju, je odabrano od 0, 1 i 2.
4. Spoj iz patentnog zahtjeva 1 koje ima Formulu:
5. Spoj iz patentnog zahtjeva 1 koje ima Formulu:
6. Spoj iz patentnog zahtjeva 1 koje ima Formulu:
7. Spoj iz patentnog zahtjeva 1 koje ima Formulu:
8. Farmaceutska kompozicija, koja sadrži farmaceutski prihvatljiv nosač i spoj kao što je definirano u bilo kojem od patentnih zahtjeva 1 do 3, ili stereoizomere, tautomere, farmaceutski prihvatljive soli, ili solvate istog, zasebno ili u kombinaciji sa drugim terapijskim agensom.
9. Farmaceutska kompozicija, koja sadrži farmaceutski prihvatljiv nosač i spoj kao što je definirano u bilo kojem od patentnih zahtjeva 4 do 7, zasebno ili u kombinaciji sa drugim terapijskim agensom.
10. Spoj kao što je definirano u bilo kojem od patentnih zahtjeva 1 do 3, ili stereoizomeri, tautomeri, farmaceutski prihvatljive soli, ili solvati istog, za primjenu u terapiji.
11. Spoj kao što je definirano u bilo kojem od patentnih zahtjeva 1 do 3, ili stereoizomeri, tautomeri, farmaceutski prihvatljive soli, ili solvati istog, za primjenu u liječenju tromboembolijskog poremećaja ili primarnoj ili sekundarnoj profilaksi tromboembolijskog poremećaja.
12. Spoj za primjenu kao što je definirano u patentnom zahtjevu 11, gdje je tromboembolijski poremećaj odabran iz grupe koja se sastoji od arterijskih kardiovaskularnih tromboembolijskih poremećaja, venskih kardiovaskularnih tromboembolijskih poremećaja, cerebrovaskularnih tromboembolijskih poremećaja, i tromboembolijskih poremećaja u komorama srca ili u perifernoj cirkulaciji.
13. Spoj kao što je definirano u bilo kojem od patentnih zahtjeva 4 do 7 za primjenu u terapiji.
14. Spoj kao što je definirano u bilo kojem od patentnih zahtjeva 4 do 7 za primjenu u liječenju tromboembolijskog poremećaja ili primarnoj ili sekundarnoj profilaksi tromboembolijskog poremećaja.
15. Spoj za primjenu kao što je definirano u patentnom zahtjevu 14, gdje tromboembolijski poremećaj je odabran iz grupe koja se sastoji od arterijskih kardiovaskularnih tromboembolijskih poremećaja, venskih kardiovaskularnih tromboembolijskih poremećaja, cerebrovaskularnih tromboembolijskih poremećaja, i tromboembolijskih poremećaja u komorama srca ili u perifernoj cirkulaciji.
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