DE102006025316A1 - Isoindolin-1-one, isoindolin-3-one and isoindoline-1,3-dione derivatives and their use - Google Patents

Abstract

The invention relates to novel isoindolin-1-one, isoindolin-3-one and isoindoline-1,3-dione derivatives, processes for their preparation, their use for the treatment and / or prophylaxis of diseases and their use for the preparation of medicaments for the treatment and / or prophylaxis of diseases, in particular thromboembolic diseases.

Description

The Invention relates to novel isoindolin-1-one, isoindolin-3-one and isoindoline-1,3-dione derivatives, Process for their preparation, their use for treatment and / or Prophylaxis of diseases and their use for the production of medicaments for the treatment and / or prophylaxis of diseases, in particular of thromboembolic diseases.

The Blood clotting is a protective mechanism of the organism with which Help defects in the vessel wall quickly and reliably "sealed" Blood loss can be avoided or minimized. The haemostasis after vascular injury takes place essentially by the coagulation system, in which a enzymatic cascade of complex reactions of plasma proteins. Numerous coagulation factors are involved, of which each, once activated, the next inactive preliminary stage in each case converts their active form. At the The end of the cascade is the conversion of the soluble fibrinogen into the insoluble Fibrin, causing a blood clot. Traditionally different one in the blood coagulation between the intrinsic and the extrinsic System in a final lead common reaction path. Here comes the factor Xa, which is formed from the proenzyme factor X. becomes, a key role too, as it connects both coagulation pathways. The activated serine protease Xa cleaves prothrombin to thrombin. The resulting thrombin turn in turn splits fibrinogen to fibrin. By subsequent cross-linking The fibrin monomers cause the formation of blood clots and thus for haemostasis. About that In addition, thrombin is a potent trigger of platelet aggregation, which also makes a significant contribution to hemostasis guaranteed.

The hemostasis is subject to a complex regulatory mechanism. An uncontrolled Activation of the coagulation system or a defective inhibition of the Activation processes can be the formation of local thrombosis or Emboli in vessels (arteries, Veins, lymph vessels) or heart caves cause. This can lead to serious thromboembolic disorders to lead. About that In addition, hypercoagulability - systemically - in a Consumption coagulopathy lead to disseminated intravascular coagulation. thromboembolic Complications also occur in microangiopathic hemolytic anemias, extracorporeal blood circuits, like hemodialysis, and heart valve prostheses.

thromboembolic Diseases are the most common Cause of morbidity and mortality in most industrialized countries [Heart Disease: A Textbook of Cardiovascular Medicine, Eugene Braunwald, 5th edition, 1997, W. B. Saunders Company, Philadelphia].

The Anticoagulants known in the art, i. matter to inhibit or prevent blood clotting, have different, often serious disadvantages. An efficient treatment method or prophylaxis of thromboembolic diseases proves in practice therefore very difficult and unsatisfactory.

For the therapy and prophylaxis of thromboembolic diseases finds on the one hand Heparin use which is administered parenterally or subcutaneously. Due to cheaper Although pharmacokinetic properties are increasing these days low molecular weight heparin is preferred; however, this can also help the known disadvantages described below are not avoided that exist in therapy with heparin. So is heparin orally ineffective and has only a comparatively low half-life. Because heparin simultaneously affects several factors of the blood coagulation cascade inhibits, it comes to an unselective effect. Furthermore there is a high risk of bleeding, especially brain bleeding and bleeding can occur in the gastrointestinal tract, and it can lead to thrombocytopenia, Alopecia medicomentosa or osteoporosis come [Pschyrembel, Clinical Dictionary, 257th edition, 1994, Walter de Gruyter Verlag, page 610, keyword "heparin"; Römpp Lexikon Chemistry, Version 1.5, 1998, Georg Thieme Verlag Stuttgart, keyword "heparin"].

A second class of anticoagulants are the vitamin K antagonists. These include, for example, 1,3-indandiones, but especially compounds such as warfarin, phenprocoumon, dicumarol and other coumarin derivatives, which are unsuitable for the synthesis of various products of certain vitamin K-dependent coagulation factors in the liver. Due to the mechanism of action, the effect is only very slow (latency until the onset 36 to 48 hours). Although the compounds can be administered orally, due to the high risk of bleeding and the narrow therapeutic index, a complex individual adjustment and observation of the patient is necessary [J. Hirsh, J. Dalen, DR Anderson et al., "Oral anticoagulants: Mechanism of action, clinical effectiveness, and optimal therapeutic range" Chest 2001, 119, 8S-21S; J. Ansell, J. Hirsh, J. Dalen et al ., "Managing oral anticoagulant therapy" Chest 2001, 119, 22S-38S; PS Wells, AM Holbrook, NR Crowther et al., "Interactions of warfarin with drugs and food" Ann., Intern., Med., 1994, 121, 676-683].

In recently, Time is a new therapeutic approach to treatment and prophylaxis have been described by thromboembolic disorders. Goal of this new therapeutic approach is the inhibition of factor Xa. Corresponding the central role factor Xa in the blood coagulation cascade Factor Xa represents one of the most important anticoagulant targets Active substances [J. Hauptmann, J. Stürzebecher, Thrombosis Research 1999, 93, 203; S.A.V. Raghavan, M. Dikshit, "Recent advances in the status and Targets of Antithrombotic Agents "Drugs Fut. 2002, 27, 669-683; H.A. Wieland, V. Laux, D. Kozian, M. Lorenz, "Approaches in Anticoagulation: Rational for target positioning "Curr. Opin. Investig .. Drugs 2003, 4, 264-271; Ú.J. Ries, W. Wienen, "Serine proteases as targets for antithrombotic therapy "Drugs Fut. 2003, 28, 355-370; L.-A. Linkins, J.I. Weitz, "New anticoagulant therapy "Annu. Rev. Med. 2005, 56, 63-77; A. Casimiro-Garcia et al., Progress in the discovery of Factor Xa inhibitors "Expert Opinion Ther. Patents 2006,15, 119-145].

there It has been shown that different, both peptidic and non-peptidic Compounds in animal models are effective as factor Xa inhibitors. A big Number of direct factor Xa inhibitors is known to date [J.M. Walenga; W. P. Jeske, D. Hoppensteadt, J. Fareed, "Factor Xa Inhibitors: Today and Beyond "Curr. Opin. Investig. Drugs 2003, 4, 272-281; J. Ruef, H.A. Katus, "New antithrombotic drugs on the horizon "Expert Opin. Investig. Drugs 2003, 12, 781-797; M.L. Quan, J.M. Smallheer, "The race to anally active Factor Xa inhibitor: Recent advances "Curr. Opin. Drug Discovery & Development 2004, 7, 460-469]. Farther are nonpeptidic, low molecular weight factor Xa inhibitors, for example also in WO 03/099276, WO 03/011858 and WO 03/007942.

A Object of the present invention is to provide new alternative compounds with comparable or improved activity, for fighting of diseases, in particular thromboembolic diseases, in humans and animals.

in welcher
A für eine Gruppe der Formel

steht,
wobei
R^1A für Wasserstoff, Fluor, Trifluormethyl, Hydroxy, Amino, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyl, C₃-C₆-Cycloalkyloxy oder C₃-C₆-Cycloalkylamino steht,
worin Alkyl, Alkoxy, Alkylamino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyloxy, C₃-C₆-Cycloalkylamino, (N-C₃-C₆-Cycloalkyl)(N-C₁-C₄-alkyl)amino und einem 4- bis 7-gliedrigen gesättigten Heterocyclus, der ein Ringglied aus der Reihe N-R²¹, S oder O enthalten kann,
worin
R²¹ für Wasserstoff, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
und
der Heterocyclus substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, C₁-C₄-Alkyl und Oxo,
R^1B für Wasserstoff, Hydroxy, Amino, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyl, C₃-C₆-Cycloalkyloxy oder C₃-C₆-Cycloalkylamino steht,
worin Alkyl substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyloxy, C₃-C₆-Cycloalkylamino, (N-C₃-C₆-Cycloalkyl)(N-C₁-C₄-alkyl)amino und einem 4- bis 7-gliedrigen gesättigten Heterocyclus, der ein Ringglied aus der Reihe N-R²¹, S oder O enthalten kann,
worin
R²¹ für Wasserstoff, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
und
der Heterocyclus substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, C₁-C₄-Alkyl und Oxo,
R^1C für Wasserstoff, Fluor, Cyano, Hydroxy, Amino, Oxo, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino oder C₃-C₆-Cycloalkyl steht,
R^1D für Wasserstoff, Fluor, Cyano, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
R^1E für Wasserstoff, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
und # die Anknüpfstelle an den Phenylring ist,
m für die Zahl 0, 1 oder 2 steht,
und die (CH₂)_m-Gruppe in 1 oder 2 Position an den Phenyl-Ring gebunden ist,
R² für Wasserstoff, Fluor, Chlor, Cyano, Hydroxy, Amino, Trifluormethyl, Trifluormethoxy, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkoxymethyl, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyl, Aminocarbonyl, C₁-C₄-Alkoxycarbonyl oder C₁-C₄-Alkylaminocarbonyl steht,
R³ für Wasserstoff, Fluor, Chlor, Cyano, Hydroxy, Amino, Trifluormethyl, Trifluormethoxy, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkoxymethyl, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyl, Aminocarbonyl, C₁-C₄-Alkoxycarbonyl oder C₁-C₄-Alkylaminocarbonyl steht,
wobei Alkyl, Alkoxy und Alkylamino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, C₁-C₄-Alkoxy, C₃-C₆-Cycloalkyloxy, Pyrrolidinyl, Piperidinyl, Morpholinyl, Piperazinyl, 4-Tetrahydropyranyl und -NR¹⁴R¹⁵,
wobei Piperazinyl und Piperidinyl am Stickstoffatom substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
und
R¹⁴ für Wasserstoff, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
und
R¹⁵ für Wasserstoff oder C₁-C₄-Alkyl steht,
R⁴ und R⁵ für Wasserstoff stehen,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ für Wasserstoff stehen,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
R⁸ für Phenyl, Pyridyl, Pyrazinyl, Pyrimidinyl, Pyridazinyl oder Thienyl steht,
wobei Phenyl, Pyridyl, Pyrazinyl, Pyrimidinyl und Pyridazinyl substituiert sind mit einem Substituenten R¹¹ und/oder einem Substituenten R¹² oder mit zwei verschiedenen Substituenten R¹¹ oder mit zwei verschiedenen Substituenten R¹²,
wobei
R¹¹ an ein Kohlenstoffatom gebunden ist, das nicht einem Stickstoffatom im Ring benachbart ist, und für Wasserstoff, Fluor, Chlor, Cyano, Ethinyl, C₁-C₄-Alkyl, C₁-C₄-Alkoxy oder C₃-C₆-Cycloalkyl steht,
R¹² an ein Kohlenstoffatom gebunden ist, das einem Stickstoffatom im Ring benachbart ist, und für Wasserstoff, Amino, C₁-C₄-Alkyl, C₁-C₄-Alkylamino oder C₃-C₆-Cycloalkyl steht,
und
wobei Thienyl substituiert ist mit einem Substituenten R¹³ und einem Substituenten R¹⁶,
wobei
R¹³ an ein Kohlenstoffatom gebunden ist, das dem Schwefelatom im Ring benachbart ist, und für Wasserstoff, Fluor, Chlor, Cyano, Ethinyl, C₁-C₄-Alkyl, C₁-C₄-Alkoxy oder C₃-C₆-Cycloalkyl steht,
R¹⁶ für Wasserstoff, Fluor, Chlor, Amino, C₁-C₄-Alkyl, C₁-C₄-Alkylamino oder C₃-C₆-Cycloalkyl steht,
R⁹ für Wasserstoff, Fluor, Chlor, Cyano, Hydroxy, Amino, Trifluormethyl, Trifluormethoxy, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkylamino, C₃-C₆-Cycloalkyl, Aminocarbonyl, C₁-C₄-Alkoxycarbonyl oder C₁-C₄-Alkylaminocarbonyl steht,
wobei Alkyl, Alkoxy und Alkylamino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, C₁-C₄-Alkoxy, C₃-C₆-Cycloalkyloxy, Pyrrolidinyl, Piperidinyl, Morpholinyl, Piperazinyl, 4-Tetrahydropyranyl und -NR¹⁷R¹⁸,
wobei Piperazinyl und Piperidinyl am Stickstoffatom substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
und
R¹⁷ für Wasserstoff, C₁-C₄-Alkyl oder C₃-C₆-Cycloalkyl steht,
und
R¹⁸ für Wasserstoff oder C₁-C₄-Alkyl steht,
R¹⁰ für Wasserstoff, Fluor, Chlor, Cyano, Trifluormethyl, Trifluormethoxy, C₁-C₄-Alkyl, C₁-C₄-Alkoxy oder C₃-C₆-Cycloalkyl steht,
und
wobei R⁹ an die 6-Position und R¹⁰ an die 7-Position des Isoindolin-Rings gebunden ist,
oder
wobei R⁹ an die 7-Position und R¹⁰ an die 6-Position des Isoindolin-Rings gebunden ist,
und ihre Salze, ihre Solvate und die Solvate ihrer Salze.The invention relates to compounds of the formula

in which
A is a group of the formula

stands,
in which
R ^{1A is} hydrogen, fluorine, trifluoromethyl, hydroxy, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, C ₃ -C ₆ Cycloalkyloxy or C ₃ -C ₆ cycloalkylamino,
wherein alkyl, alkoxy, alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ alkoxy, C ₁ -C ₄ alkylamino, C ₃ -C ₆ cycloalkyloxy , C ₃ -C ₆ -cycloalkylamino, (NC ₃ -C ₆ -cycloalkyl) (NC ₁ -C ₄ -alkyl) -amino and a 4- to 7-membered saturated heterocycle which is a ring member from the series NR ²¹ , S or O may contain
wherein
R ^{21 is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
and
the heterocycle may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ -alkyl and oxo,
R ^{1B is} hydrogen, hydroxy, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, C ₃ -C ₆ -cycloalkyloxy or C C ₃ -C ₆ -cycloalkylamino,
wherein alkyl may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ alkoxy, C ₁ -C ₄ alkylamino, C ₃ -C ₆ cycloalkyloxy, C ₃ - C ₆ -cycloalkylamino, (NC ₃ -C ₆ -cycloalkyl) (NC ₁ -C ₄ -alkyl) -amino and a 4- to 7-membered saturated heterocycle which may contain a ring member from the series NR ²¹ , S or O,
wherein
R ^{21 is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
and
the heterocycle may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ -alkyl and oxo,
R ^{1C is} hydrogen, fluorine, cyano, hydroxyl, amino, oxo, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino or C ₃ -C ₆ -cycloalkyl,
R ^{1D is} hydrogen, fluorine, cyano, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
R ^{1E is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
and # is the point of attachment to the phenyl ring,
m is the number 0, 1 or 2,
and the (CH ₂ ) _m group is attached to the phenyl ring in 1 or 2 position,
R ^{2 is} hydrogen, fluorine, chlorine, cyano, hydroxyl, amino, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino , C ₃ -C ₆ -cycloalkyl, aminocarbonyl, C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl,
R ^{3 is} hydrogen, fluorine, chlorine, cyano, hydroxyl, amino, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino , C ₃ -C ₆ -cycloalkyl, aminocarbonyl, C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl,
wherein alkyl, alkoxy and alkylamino may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, C ₁ -C ₄ alkoxy, C ₃ -C ₆ cycloalkyloxy, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, 4 Tetrahydropyranyl and -NR ¹⁴ R ¹⁵ ,
wherein piperazinyl and piperidinyl may be substituted on the nitrogen atom with a substituent, wherein the substituent is selected from the group consisting of methyl and cyclopropyl,
and
R ^{14 is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
and
R ^{15 is} hydrogen or C ₁ -C ₄ -alkyl,
R ⁴ and R ^{5 are} hydrogen,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ^{7 are} hydrogen,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
R ^{8 is} phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl or thienyl,
where phenyl, pyridyl, pyrazinyl, pyrimidinyl and pyridazinyl are substituted by one substituent R ¹¹ and / or one substituent R ¹² or by two different substituents R ¹¹ or by two different substituents R ¹² ,
in which
R ¹¹ is bonded to a carbon atom which is not adjacent to a nitrogen atom in the ring, and is hydrogen, fluorine, chlorine, cyano, ethynyl, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy or C ₃ -C ₆ Cycloalkyl,
R ¹² is bonded to a carbon atom adjacent to a nitrogen atom in the ring and is hydrogen, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkylamino or C ₃ -C ₆ -cycloalkyl,
and
where thienyl is substituted by a substituent R ¹³ and a substituent R ¹⁶ ,
in which
R ^{13 is} attached to a carbon atom adjacent to the sulfur atom in the ring, and hydrogen, Is fluorine, chlorine, cyano, ethynyl, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy or C ₃ -C ₆ -cycloalkyl,
R ^{16 is} hydrogen, fluorine, chlorine, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkylamino or C ₃ -C ₆ -cycloalkyl,
R ^{9 represents} hydrogen, fluorine, chlorine, cyano, hydroxyl, amino, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl , Aminocarbonyl, C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl,
wherein alkyl, alkoxy and alkylamino may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, C ₁ -C ₄ alkoxy, C ₃ -C ₆ cycloalkyloxy, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, 4 Tetrahydropyranyl and -NR ¹⁷ R ¹⁸ ,
wherein piperazinyl and piperidinyl may be substituted on the nitrogen atom with a substituent, wherein the substituent is selected from the group consisting of methyl and cyclopropyl,
and
R ^{17 is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl,
and
R ^{18 is} hydrogen or C ₁ -C ₄ -alkyl,
R ^{10 represents} hydrogen, fluorine, chlorine, cyano, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy or C ₃ -C ₆ -cycloalkyl,
and
wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring,
or
wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring,
and their salts, their solvates, and the solvates of their salts.

Compounds of the invention are the compounds of formula (I) and their salts, solvates and solvates the salts comprising the compounds of formula (I) below formulas and their salts, solvates and solvates of the salts as well as those of formula (I), hereinafter referred to as exemplary embodiments mentioned compounds and their salts, solvates and solvates of Salts, as far as those of formula (I), hereinafter not already mentioned salts, solvates and solvates salts.

The Compounds of the invention can dependent on of their structure in stereoisomeric forms (enantiomers, diastereomers) exist. The invention therefore includes the enantiomers or Diastereomers and their respective mixtures. From such mixtures enantiomers and / or diastereomers can be the stereoisomer isolate uniform components in a known manner.

Provided the compounds of the invention can occur in tautomeric forms, For example, the present invention encompasses all tautomeric forms.

When Salts are physiologically acceptable in the context of the present invention Salts of the compounds of the invention prefers. Also included are salts that are suitable for pharmaceutical applications themselves are not suitable, but for example for insulation or cleaning the compounds of the invention can be used.

physiological Safe salts of the compounds of the invention include acid addition salts of mineral acids, carboxylic acids and sulfonic acids, e.g. Salts of hydrochloric acid, hydrobromic, Sulfuric acid, Phosphoric acid, methane, ethanesulfonic, toluene sulfonic acid, benzenesulfonic, naphthalenedisulfonic, Acetic acid, trifluoroacetic, propionic acid, Lactic acid Tartaric acid, malic acid, citric acid, fumaric acid, maleic acid and Benzoic acid.

physiological acceptable salts of the compounds of the invention also include Salts more usual Bases, such as by way of example and preferably alkali metal salts (e.g. Sodium and potassium salts), alkaline earth salts (e.g., calcium and magnesium salts) and ammonium salts derived from ammonia or organic amines with 1 to 16 carbon atoms, such as by way of example and preferably ethylamine, Diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, Diethanolamine, triethanolamine, dicyclohexylamine, dimethylaminoethanol, procaine, Dibenzylamine, N-methylmorpholine, arginine, lysine, ethylenediamine and N-methylpiperidine.

When In the context of the invention, solvates are those forms of the compounds according to the invention, which in solid or liquid Condition by coordination with solvent molecules a complex form. Hydrates are a special form of solvates in which the coordination with water takes place. As solvates are in the frame Hydrate is preferred in the present invention.

It also includes the present invention also prodrugs of the compounds of the invention. Of the Term "prodrugs" includes compounds, which may themselves be biologically active or inactive, but during their Residence time in the body to compounds of the invention be implemented (for example, metabolically or hydrolytically).

Unless otherwise specified, in the context of the present invention, the substituents have the following meaning:
Alkyl per se and "Alk" and "alkyl" in alkoxy Alkylamino Alkoxycarbonyl Alkylaminocarbonyl, alkylcarbonylamino and alkoxycarbonylamino represent a linear or branched alkyl radical having usually 1 to 4, preferably 1 or 2 carbon atoms, by way of example and preferably methyl, ethyl, n -Propyl, isopropyl and tert-butyl.

alkoxy is exemplary and preferably methoxy, ethoxy, n-propoxy, Isopropoxy and tert-butoxy.

Alkylamino represents an alkylamino radical having one or two (independently selected) alkyl substituents, by way of example and by way of preference methylamino, ethylamino, n-propylamino, isopropylamino, tert-butylamino, N, N-dimethylamino, N, N-diethylamino, N-ethyl N-methylamino, N-methyl-Nn-propylamino, N-isopropyl-Nn-propylamino and N-tert-butyl-N-methylamino. C ₁ -C ₃ -alkylamino is, for example, a monoalkylamino radical having 1 to 3 carbon atoms or a dialkylamino radical having in each case 1 to 3 carbon atoms per alkyl substituent.

alkoxycarbonyl is exemplary and preferably methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl and tert-butoxycarbonyl.

Alkylaminocarbonyl represents an alkylaminocarbonyl radical having one or two (independently selected) alkyl substituents, by way of example and preferably methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl, tert-butylaminocarbonyl, N, N-dimethylaminocarbonyl, N, N-diethylaminocarbonyl, N Ethyl-N-methylaminocarbonyl, N-methyl-Nn-propylaminocarbonyl, N-isopropyl-Nn-propylaminocarbonyl and N-tert-butyl-N-methylaminocarbonyl. C ₁ -C ₃ -alkylaminocarbonyl is, for example, a monoalkylaminocarbonyl radical having 1 to 3 carbon atoms or a dialkylaminocarbonyl radical having in each case 1 to 3 carbon atoms per alkyl substituent.

alkylcarbonylamino is exemplary and preferably methylcarbonylamino, ethylcarbonylamino, n-propylcarbonylamino, isopropylcarbonylamino and tert-butylcarbonylamino.

alkoxycarbonylamino is exemplary and preferably methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino, isopropoxycarbonylamino and tert-butoxycarbonylamino.

cycloalkyl stands for a cycloalkyl group of usually 3 to 6 carbon atoms, preferably having 3 to 5 carbon atoms, by way of example and preferably for cyclopropyl, Cyclobutyl, cyclopentyl and cyclohexyl.

Heterocyclyl is a monocyclic, heterocyclic radical having usually 4 to 7 ring atoms and up to 3, preferably up to 2 heteroatoms and / or hetero groups from the series N, O, S, SO, SO ₂ . The heterocyclyl radicals may be saturated or partially unsaturated. Preference is given to 5- to 7-membered, monocyclic saturated heterocyclyl radicals having up to two heteroatoms from the series O, N and S, such as by way of example and preferably tetrahydrofuranyl, pyrrolidinyl, pyrrolinyl, piperidinyl, tetrahydropyranyl, piperazinyl, morpholinyl and perhydroazepinyl.

heteroaryl stands for an aromatic, monocyclic radical having 5 or 6 ring atoms and up to 4 heteroatoms from the series S, O and N, by way of example and preferably for Thienyl, furyl, pyrrolyl, thiazolyl, oxazolyl, isoxazolyl, isothiazolyl, Imidazolyl, pyrazolyl, pyridyl, pyrimidinyl, pyridazinyl and pyrazinyl.

If Residues in the compounds of the invention may be substituted the radicals, unless otherwise specified, one or more times be substituted. In the context of the present invention, for all radicals, which occur multiple times, whose meaning is independent of each other. A Substitution with one, two or three equal or different Substituents are preferred. Most preferably, the substitution with a substituent.

In the formulas of the group which may stand for A, the endpoint of the line next to each of which represents a # does not represent a carbon atom or a CH ₂ group but is part of the bond to the atom to which A is attached.

In the formulas of the group which can stand for R ⁸ , the end point of the line next to each one * does not stand for a carbon atom or a CH ₂ group but is part of the bond to the atom to which R ^{5 is} attached is.

steht,
wobei
R^1A für Wasserstoff, Fluor, Hydroxy, Amino, C₁-C₄-Alkyl, Methoxy, Ethoxy, tert.-Butoxy, Methylamino, Dimethylamino, Ethylamino, Diethylamino, tert.-Butyl-amino, Cyclopropyl, Cyclopropylamino oder Cyclopropyloxy steht,
worin Alkyl, Ethoxy, tert.-Butoxy, Ethylamino, Diethylamino und tert.-Butyl-amino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, Methoxy, C₁-C₄-Alkylamino, Cyclopropyloxy, Cyclopropylamino, (N-Cyclopropyl)(N-methyl)amino, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Piperidinyl, 4-Morpholinyl, 1-Piperazinyl und 4-Tetrahydropyranyl,
wobei 1-Piperazinyl und 4-Piperidinyl am Stickstoffatom substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
R^1B für Wasserstoff, Hydroxy, Amino, C₁-C₄-Alkyl, Methoxy, Methylamino, Dimethylamino oder Cyclopropyl steht,
worin Alkyl substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, Methoxy, C₁-C₄-Alkylamino, Cyclopropyloxy, Cyclopropylamino, (N-Cyclopropyl)(N-methyl)amino, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Piperidinyl, 4-Morpholinyl, 1-Piperazinyl und 4-Tetrahydropyranyl,
wobei 1-Piperazinyl und 4-Piperidinyl am Stickstoffatom substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
R^1C für Wasserstoff, Fluor, Oxo oder Methyl steht,
R^1D für Wasserstoff, Fluor oder Methyl steht,
und # die Anknüpfstelle an den Phenylring ist,
m für die Zahl 0, 1 oder 2 steht,
und die (CH₂)_m-Gruppe in 1 oder 2 Position an den Phenyl-Ring gebunden ist,
R² für Wasserstoff, Fluor, Chlor, Cyano, Hydroxy, C₁-C₄-Alkyl oder C₁-C₄-Alkoxy steht,
R³ für Wasserstoff, Fluor, Chlor, Cyano, Hydroxy, C₁-C₄-Alkyl, C₁-C₄-Alkoxy, C₁-C₄-Alkoxymethyl, C₁-C₄-Alkylamino, Cyclopropyl, Aminocarbonyl, C₁-C₄-Alkoxycarbonyl oder C₁-C₄-Alkylaminocarbonyl steht,
wobei Alkyl, Alkoxy und Alkylamino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Methoxy, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Morpholinyl, 1-Piperazinyl und -NR¹⁴R¹⁵,
wobei 1-Piperazinyl am Stickstoffatom substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
und
R¹⁴ für Wasserstoff, Methyl oder Cyclopropyl steht,
und
R¹⁵ für Wasserstoff oder Methyl steht,
R⁴ und R⁵ für Wasserstoff stehen,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ für Wasserstoff stehen,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
R⁸ für eine Gruppe der Formel

steht,
wobei
* die Anknüpfstelle an die Carbonylgruppe ist,
R¹¹ für Fluor, Chlor, Ethinyl, Methyl, Ethyl, Methoxy oder Ethoxy steht,
R¹² für Amino, Methyl, Methylamino oder Dimethylamino steht,
R¹³ für Fluor, Chlor, Ethinyl, Methyl, Ethyl, Methoxy oder Ethoxy steht,
und
R¹⁶ für Wasserstoff steht,
R⁹ für Wasserstoff, Fluor, Chlor, Cyano, Methyl, Methoxy, Aminocarbonyl, Methylaminocarbonyl oder Dimethylaminocarbonyl steht,
wobei Methyl und Methoxy substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Methoxy, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Morpholinyl, 1-Piperazinyl und -NR¹⁷R^18,
wobei 1-Piperazinyl am Stickstoffatom substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
und
R¹⁷ für Wasserstoff, Methyl oder Cyclopropyl steht,
und
R^1B für Wasserstoff oder Methyl steht,
R¹⁰ für Wasserstoff, Fluor, Chlor, Cyano, Trifluormethyl, Trifluormethoxy, Methyl oder Methoxy steht,
und
wobei R⁹ an die 6-Position und R¹⁰ an die 7-Position des Isoindolin-Rings gebunden ist,
oder
wobei R⁹ an die 7-Position und R¹⁰ an die 6-Position des Isoindolin-Rings gebunden ist,
und ihre Salze, ihre Solvate und die Solvate ihrer Salze.Preference is given to compounds of the formula (I) in which
A is a group of the formula

stands,
in which
R ^{1A represents} hydrogen, fluorine, hydroxyl, amino, C ₁ -C ₄ -alkyl, methoxy, ethoxy, tert-butoxy, methylamino, dimethylamino, ethylamino, diethylamino, tert-butyl-amino, cyclopropyl, cyclopropylamino or cyclopropyloxy,
wherein alkyl, ethoxy, tert-butoxy, ethylamino, diethylamino and tert-butyl-amino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, methoxy, C ₁ -C ₄ alkylamino , Cyclopropyloxy, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1-pyrrolidinyl, 1-piperidinyl, 4-piperidinyl, 4-morpholinyl, 1-piperazinyl and 4-tetrahydropyranyl,
wherein 1-piperazinyl and 4-piperidinyl may be substituted on the nitrogen atom with a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
R ^{1B is} hydrogen, hydroxy, amino, C ₁ -C ₄ -alkyl, methoxy, methylamino, dimethylamino or cyclopropyl,
wherein alkyl may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, amino, methoxy, C ₁ -C ₄ alkylamino, cyclopropyloxy, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1 Pyrrolidinyl, 1-piperidinyl, 4-piperidinyl, 4-morpholinyl, 1-piperazinyl and 4-tetrahydropyranyl,
wherein 1-piperazinyl and 4-piperidinyl may be substituted on the nitrogen atom with a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
R ^{1C is} hydrogen, fluorine, oxo or methyl,
R ^{1D is} hydrogen, fluorine or methyl,
and # is the point of attachment to the phenyl ring,
m is the number 0, 1 or 2,
and the (CH ₂ ) _m group is attached to the phenyl ring in 1 or 2 position,
R ^{2 is} hydrogen, fluorine, chlorine, cyano, hydroxy, C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy,
R ^{3 is} hydrogen, fluorine, chlorine, cyano, hydroxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino, cyclopropyl, aminocarbonyl, C C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl,
wherein alkyl, alkoxy and alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, methoxy, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, 1-piperazinyl and -NR ¹⁴ R ¹⁵ ,
where 1-piperazinyl may be substituted on the nitrogen atom by a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
and
R ^{14 is} hydrogen, methyl or cyclopropyl,
and
R ^{15 is} hydrogen or methyl,
R ⁴ and R ^{5 are} hydrogen,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ^{7 are} hydrogen,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
R ^{8 is} a group of the formula

stands,
in which
* is the point of attachment to the carbonyl group,
R ^{11 is} fluorine, chlorine, ethynyl, methyl, ethyl, methoxy or ethoxy,
R ^{12 is} amino, methyl, methylamino or dimethylamino,
R ^{13 is} fluorine, chlorine, ethynyl, methyl, ethyl, methoxy or ethoxy,
and
R ^{16 is} hydrogen,
R ^{9 represents} hydrogen, fluorine, chlorine, cyano, methyl, methoxy, aminocarbonyl, methylaminocarbonyl or dimethylaminocarbonyl,
wherein methyl and methoxy may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, methoxy, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, 1-piperazinyl and -NR ¹⁷ R ^18,
where 1-piperazinyl may be substituted on the nitrogen atom by a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
and
R ^{17 is} hydrogen, methyl or cyclopropyl,
and
R ^{1B is} hydrogen or methyl,
R ^{10 is} hydrogen, fluorine, chlorine, cyano, trifluoromethyl, trifluoromethoxy, methyl or methoxy,
and
wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring,
or
wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring,
and their salts, their solvates, and the solvates of their salts.

steht,
wobei
R^1A für Wasserstoff, Fluor, Hydroxy, Amino, Methyl, Ethyl, iso-Propyl, Methoxy, Ethoxy, Methylamino, Dimethylamino, Ethylamino, Diethylamino oder Cyclopropylamino steht,
worin Methyl, Ethyl, iso-Propyl, Ethoxy, Ethylamino und Diethylamino substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, Methoxy, Methylamino, Dimethylamino, Cyclopropylamino, (N-Cyclopropyl)(N-methyl)amino, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Morpholinyl und 1-Piperazinyl,
wobei 1-Piperazinyl am Stickstoffatom substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
R^1B für Wasserstoff, Hydroxy, Amino, Methyl, Ethyl, iso-Propyl oder Cyclopropyl steht,
worin Ethyl und iso-Propyl substituiert sein können mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Hydroxy, Amino, Methoxy, Methylamino, Dimethylamino, Cyclopropylamino, (N-Cyclopropyl)(N-methyl)amino, 1-Pyrrolidinyl, 1-Piperidinyl, 4-Morpholinyl und 1-Piperazinyl,
wobei 1-Piperazinyl am Stickstoffatom substituiert sein kann mit einem Substituenten, wobei der Substituent ausgewählt wird aus der Gruppe bestehend aus Methyl und Cyclopropyl,
R^1C für Wasserstoff, Fluor, Oxo oder Methyl steht,
R^1D für Wasserstoff, Fluor oder Methyl steht,
und # die Anknüpfstelle an den Phenylring ist,
m für die Zahl 1 steht,
und die (CH₂)_m-Gruppe in 1 oder 2 Position an den Phenyl-Ring gebunden ist,
R² für Wasserstoff steht,
R³ für Wasserstoff, Fluor, Chlor, Cyano, Methyl, Ethyl, n-Propyl, Methoxy, Ethoxy oder Methoxymethyl steht,
R⁴ und R⁵ für Wasserstoff stehen,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ für Wasserstoff stehen,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
R⁸ für eine Gruppe der Formel

steht,
wobei
* die Anknüpfstelle an die Carbonylgruppe ist,
R¹³ für Fluor, Chlor oder Methyl steht,
und
R¹⁶ für Wasserstoff steht,
R⁹ für Wasserstoff steht,
R¹⁰ für Wasserstoff steht,
und
wobei R⁹ an die 6-Position und R¹⁰ an die 7-Position des Isoindolin-Rings gebunden ist,
oder
wobei R⁹ an die 7-Position und R¹⁰ an die 6-Position des Isoindolin-Rings gebunden ist,
und ihre Salze, ihre Solvate und die Solvate ihrer Salze.Preference is also given to compounds of the formula (I) in which
A is a group of the formula

stands,
in which
R ^{1A represents} hydrogen, fluorine, hydroxyl, amino, methyl, ethyl, isopropyl, methoxy, ethoxy, methylamino, dimethylamino, ethylamino, diethylamino or cyclopropylamino,
wherein methyl, ethyl, iso-propyl, ethoxy, ethylamino and diethylamino may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, amino, methoxy, methylamino, dimethylamino, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl and 1-piperazinyl,
where 1-piperazinyl may be substituted on the nitrogen atom by a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
R ^{1B is} hydrogen, hydroxy, amino, methyl, ethyl, iso-propyl or cyclopropyl,
wherein ethyl and iso-propyl may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, amino, methoxy, methylamino, dimethylamino, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1-pyrrolidinyl , 1-piperidinyl, 4-morpholinyl and 1-piperazinyl,
where 1-piperazinyl may be substituted on the nitrogen atom by a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl,
R ^{1C is} hydrogen, fluorine, oxo or methyl,
R ^{1D is} hydrogen, fluorine or methyl,
and # is the point of attachment to the phenyl ring,
m is the number 1,
and the (CH ₂ ) _m group is attached to the phenyl ring in 1 or 2 position,
R ^{2 is} hydrogen,
R ^{3 is} hydrogen, fluorine, chlorine, cyano, methyl, ethyl, n-propyl, methoxy, ethoxy or methoxymethyl,
R ⁴ and R ^{5 are} hydrogen,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ^{7 are} hydrogen,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
R ^{8 is} a group of the formula

stands,
in which
* is the point of attachment to the carbonyl group,
R ^{13 is} fluorine, chlorine or methyl,
and
R ^{16 is} hydrogen,
R ^{9 is} hydrogen,
R ^{10 is} hydrogen,
and
wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring,
or
wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring,
and their salts, their solvates, and the solvates of their salts.

steht,
wobei
# die Anknüpfstelle an den Phenylring ist,
m für die Zahl 1 steht,
und die (CH₂)_m-Gruppe in 1 oder 2 Position an den Phenyl-Ring gebunden ist,
R² für Wasserstoff steht,
R³ für Wasserstoff, Fluor, Chlor, Cyano oder Methyl steht,
R⁴ und R⁵ für Wasserstoff stehen,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ für Wasserstoff stehen,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
R⁸ für eine Gruppe der Formel

steht,
wobei
* die Anknüpfstelle an die Carbonylgruppe ist,
R¹³ für Chlor steht,
und
R¹⁶ für Wasserstoff steht,
R⁹ für Wasserstoff steht,
R¹⁰ für Wasserstoff steht,
und
wobei R⁹ an die 6-Position und R¹⁰ an die 7-Position des Isoindolin-Rings gebunden ist,
oder
wobei R⁹ an die 7-Position und R¹⁰ an die 6-Position des Isoindolin-Rings gebunden ist,
und ihre Salze, ihre Solvate und die Solvate ihrer Salze.Preference is also given to compounds of the formula (I) in which
A is a group of the formula

stands,
in which
# is the point of attachment to the phenyl ring,
m is the number 1,
and the (CH ₂ ) _m group is attached to the phenyl ring in 1 or 2 position,
R ^{2 is} hydrogen,
R ^{3 is} hydrogen, fluorine, chlorine, cyano or methyl,
R ⁴ and R ^{5 are} hydrogen,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ^{7 are} hydrogen,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
R ^{8 is} a group of the formula

stands,
in which
* is the point of attachment to the carbonyl group,
R ^{13 is} chlorine,
and
R ^{16 is} hydrogen,
R ^{9 is} hydrogen,
R ^{10 is} hydrogen,
and
wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring,
or
wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring,
and their salts, their solvates, and the solvates of their salts.

steht,
wobei
# die Anknüpfstelle an den Phenylring ist,
m für die Zahl 1 steht,
und die (CH₂)_m-Gruppe in 1 oder 2 Position an den Phenyl-Ring gebunden ist,
R² für Wasserstoff steht,
R³ für Wasserstoff, Fluor, Chlor, Cyano oder Methyl steht,
R⁴ und R⁵ für Wasserstoff stehen,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ für Wasserstoff stehen,
oder
R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
und
R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden,
R⁸ für eine Gruppe der Formel

steht,
wobei
* die Anknüpfstelle an die Carbonylgruppe ist,
R¹³ für Chlor steht,
und
R¹⁶ für Wasserstoff steht,
R⁹ für Wasserstoff steht,
R¹⁰ für Wasserstoff steht,
und
wobei R⁹ an die 6-Position und R¹⁰ an die 7-Position des Isoindolin-Rings gebunden ist,
oder
wobei R⁹ an die 7-Position und R¹⁰ an die 6-Position des Isoindolin-Rings gebunden ist,
und ihre Salze, ihre Solvate und die Solvate ihrer Salze.Preference is also given to compounds of the formula (I) in which
A is a group of the formula

stands,
in which
# is the point of attachment to the phenyl ring,
m is the number 1,
and the (CH ₂ ) _m group is attached to the phenyl ring in 1 or 2 position,
R ^{2 is} hydrogen,
R ^{3 is} hydrogen, fluorine, chlorine, cyano or methyl,
R ⁴ and R ^{5 are} hydrogen,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ^{7 are} hydrogen,
or
R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group,
and
R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group,
R ^{8 is} a group of the formula

stands,
in which
* is the point of attachment to the carbonyl group,
R ^{13 is} chlorine,
and
R ^{16 is} hydrogen,
R ^{9 is} hydrogen,
R ^{10 is} hydrogen,
and
wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring,
or
wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring,
and their salts, their solvates, and the solvates of their salts.

steht, wobei # die Anknüpfstelle an den Phenylring ist.Preference is also given to compounds of the formula (I) in which A is a group of the formula

where # is the point of attachment to the phenyl ring.

steht, wobei # die Anknüpfstelle an den Phenylring ist.Preference is also given to compounds of the formula (I) in which A is a group of the formula

where # is the point of attachment to the phenyl ring.

steht, wobei # die Anknüpfstelle an den Phenylring ist.Preference is also given to compounds of the formula (I) in which A is a group of the formula

where # is the point of attachment to the phenyl ring.

Prefers are also compounds of formula (I) in which m is the number 1 stands.

Preference is also given to compounds of the formula (I) in which R ^{2 is} hydrogen.

Preference is also given to compounds of the formula (I) in which R ^{3 is} hydrogen, fluorine, chlorine, cyano or methyl.

Preference is also given to compounds of the formula (I) in which R ^{3 is} hydrogen.

Preference is also given to compounds of the formula (I) in which R ² and R ^{3 are} hydrogen.

steht, wobei * die Anknüpfstelle an die Carbonylgruppe ist, R¹³ für Chlor steht und R¹⁶ für Wasserstoff steht.Preference is also given to compounds of the formula (I) in which R ^{8 is} a group of the formula

where * is the point of attachment to the carbonyl group, R ^{13 is} chlorine and R ^{16 is} hydrogen.

Preference is also given to compounds of the formula (I) in which R ⁹ and R ^{10 are} hydrogen. The residue definitions given in detail in the respective combinations or preferred combinations of residues are also replaced by residue definitions of other combinations, regardless of the particular combinations of the residues indicated.

All Particularly preferred are combinations of two or more of above preferred ranges.

• [A] die Verbindungen der Formel
  
  in welcher m, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ und R¹⁰ die oben angegebene Bedeutung haben, mit Verbindungen der Formel A-H (III),in welcher A die oben angegebene Bedeutung hat, umgesetzt werden, oder
• [B] die Verbindungen der Formel
  
  in welcher R⁸, R⁹ und R¹⁰ die oben angegebene Bedeutung haben, mit Verbindungen der Formel
  

in welcher A, m, R² und R³ die oben angegebene Bedeutung haben, zu Verbindungen der Formel (I), in welcher R⁴ und R⁵ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden, und R⁶ und R⁷ zusammen mit dem Kohlenstoffatom, an das sie gebunden sind, eine Carbonylgruppe bilden, umgesetzt werden.The invention further provides a process for the preparation of the compounds of the formula (I), or their salts, their solvates or the solvates of their salts, wherein

• [A] the compounds of the formula
  
  in which m, R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} the abovementioned meaning, with compounds of the formula AH (III), in which A has the meaning given above, or
• [B] the compounds of the formula
  
  in which R ⁸ , R ⁹ and R ^{10 have} the abovementioned meaning, with compounds of the formula
  

in which A, m, R ² and R ^{3 have} the abovementioned meaning, to compounds of the formula (I) in which R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ⁷ are reacted together with the carbon atom to which they are attached to form a carbonyl group.

The Free base of the salts can be obtained, for example, by chromatography a reversed phase column with an acetonitrile-water gradient with the addition of a base especially by using a RP18 Phenomenex Luna C18 (2) column and diethylamine as the base, or by dissolving the salts in an organic solvent and shaking with watery solutions of basic salts such as sodium bicarbonate.

Another The invention relates to a process for the preparation of the compounds of the formula (I) or its solvates in which salts of the compounds or solvates of the salts of the compounds by chromatography Addition of a base are converted into the compounds.

The Reaction according to process [A] is generally carried out in inert solvents with the addition of a copper (I) salt, a base and a diamine ligand, preferably in a temperature range of 60 ° C until the reflux of the solvent at normal pressure.

inert solvent are, for example, aprotic solvents such as toluene, dioxane, tetrahydrofuran or dimethylformamide is dioxane.

Copper (I) salts are, for example, copper (I) iodide, copper (I) chloride or copper (I) oxide, preferred is copper (I) iodide.

bases are, for example, potassium phosphate, potassium carbonate or cesium carbonate, preferred is potassium phosphate.

Diamine ligands For example, 1,2-diamines such as N, N'-dimethylethylenediamine.

The Reaction according to process [B] is generally carried out in inert solvents, in the presence of a base, preferably in a temperature range of 60 ° C to to the reflux of the solvent at normal pressure.

inert solvent For example, ethers such as dioxane or tetrahydrofuran are preferred is dioxane.

bases are, for example, amine bases such as triethylamine or diisopropylethylamine, preferred is diisopropylethylamine.

The Compounds of formulas (III), (IV) and (V) are known or are allowed according to known methods from the corresponding starting compounds synthesize.

in welcher m, R² und R³ die oben angegebene Bedeutung haben,
umgesetzt werden.The compounds of the formula (IIa) in which R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, are known or can be prepared by reacting compounds of the formula (IV) with compounds of the formula

in which m, R ² and R ^{3 have} the abovementioned meaning,
be implemented.

The Reaction takes place under the same reaction conditions as the reaction the compounds of the formula (IV) with compounds of the formula (V) (Method [B]).

The Compounds of formula (VI) are known or can be after known methods from the corresponding starting compounds synthesize.

in welcher R⁸, R⁹ und R¹⁰ die oben angegebene Bedeutung haben,
mit Verbindungen der Formel

in welcher m, R² und R³ die oben angegebene Bedeutung haben,
unter Mitsunobu-Reaktionsbedingungen umgesetzt werden.In an alternative method, the compounds of formula (IIa) can be prepared by reacting compounds of formula

in which R ⁸ , R ⁹ and R ^{10 have} the abovementioned meaning,
with compounds of the formula

in which m, R ² and R ^{3 have} the abovementioned meaning,
be implemented under Mitsunobu reaction conditions.

The Implementation is generally carried out in inert solvents, preferably in a temperature range from -20 ° C to 40 ° C at atmospheric pressure.

inert solvent For example, tetrahydrofuran, methylene chloride, dioxane or Dimethylformamide, preferred is tetrahydrofuran.

The Compounds of formulas (VII) and (VIII) are known or are allowed according to known methods from the corresponding starting compounds synthesize.

in welchen m, R², R³, R⁸, R⁹ und R¹⁰ die oben angegebene Bedeutung haben,
umgesetzt werden,
die Isomere (IXb) und (IXc) durch Kristallisation oder Chromatographie getrennt werden, und anschließend jedes Isomer einzeln in der zweiten Stufe mit Trifluoressigsäure und Triethylsilan zu der Verbindung der Formel (IIb) oder der Verbindung der Formel (IIc) umgesetzt wird.The compounds of the formula (IIb) in which R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group and R ⁶ and R ^{7 are} hydrogen, and the compounds of the formula (IIc) in which R ⁴ and R ^{5 are} hydrogen and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group are known or can be prepared by adding in the first stage compounds of formula (IIa) with a borohydride a mixture of the compounds of the formulas

in which m, R ² , R ³ , R ⁸ , R ⁹ and R ^{10 have} the abovementioned meaning,
to be implemented
the isomers (IXb) and (IXc) are separated by crystallization or chromatography, and then each isomer is individually reacted in the second step with trifluoroacetic acid and triethylsilane to the compound of formula (IIb) or the compound of formula (IIc).

The Implementation of the first stage is generally carried out in inert solvents, preferably in a temperature range from -20 ° C to 50 ° C at atmospheric pressure.

borohydrides For example, sodium borohydride or lithium borohydride are preferred is sodium borohydride.

inert solvent For example, halogenated hydrocarbons such as methylene chloride or trichloromethane, alcohols such as methanol, ethanol, n-propanol or isopropanol, or ethers, such as diethyl ether, dioxane or tetrahydrofuran, or mixtures of these solvents, preferred is a mixture of methanol and methylene chloride.

The Implementation of the second stage is generally carried out in inert solvents, preferably in a temperature range from -20 ° C to 50 ° C at atmospheric pressure.

inert solvent For example, halogenated hydrocarbons such as methylene chloride or trichloromethane, preferred is methylene chloride.

in welcher R⁹ und R¹⁰ die oben angegebene Bedeutung haben, und
R¹⁹ für Methyl oder Ethyl steht,
in der ersten Stufe mit Verbindungen der Formel (VI) umgesetzt werden,
in der zweiten Stufe die Nitrogruppe reduziert wird und
in der dritten Stufe mit Verbindungen der Formel

in welcher R⁸ die oben angegebene Bedeutung hat, und
X für Halogen, bevorzugt Brom oder Chlor, oder Hydroxy steht,
umgesetzt werden.In an alternative method, the compounds of formula (IIb) can be prepared by reacting compounds of formula

in which R ⁹ and R ^{10 have} the abovementioned meaning, and
R ^{19 is} methyl or ethyl,
in the first stage are reacted with compounds of the formula (VI),
in the second stage the nitro group is reduced and
in the third step with compounds of the formula

in which R ^{8 has} the meaning given above, and
X is halogen, preferably bromine or chlorine, or hydroxy,
be implemented.

The Reaction takes place under the same reaction conditions as the reaction the compounds of the formula (IV) with compounds of the formula (V) (Method [B]).

The Reduction of the nitro group in the second stage generally occurs with a reducing agent in inert solvents, preferably in a temperature range from room temperature to the reflux of the solvents at normal pressure up to 3 bar.

reducing agent are, for example, palladium on activated carbon and hydrogen, tin dichloride or titanium trichloride, preferably palladium on activated carbon and Hydrogen or tin dichloride.

inert solvent are, for example, ethers, such as diethyl ether, methyl tert-butyl ether, 1,2-dimethoxyethane, Dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, Alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, Hydrocarbons such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents such as dimethylformamide, dimethylacetamide, acetonitrile or pyridine, as a solvent are preferably methanol, ethanol, isopropanol or in the case of Tin dichloride in dimethylformamide.

If in the third stage X for Is halogen, the reaction is generally carried out in inert solvents, optionally in the presence of a base, preferably in a temperature range from -30 ° C to 50 ° C at atmospheric pressure.

inert solvent For example, tetrahydrofuran, methylene chloride, pyridine, dioxane or dimethylformamide, pyridine or dimethylformamide is preferred.

When inert solvent Tetrahydrofuran or methylene chloride are preferred.

bases are, for example, triethylamine, diisopropylethylamine or N-methylmorpholine, preferred is diisopropylethylamine.

If in the third stage X for Hydroxy, the reaction is generally carried out in inert solvents, in the presence of a dehydrating reagent, optionally in Presence of a base, preferably in a temperature range from -30 ° C to 50 ° C at atmospheric pressure.

inert solvent For example, halogenated hydrocarbons such as dichloromethane or trichloromethane, hydrocarbon such as benzene, nitromethane, Dioxane, dimethylformamide or acetonitrile. It is also possible to mix the solvent use. Particularly preferred is dichloromethane or dimethylformamide.

Examples of suitable dehydrating reagents are carbodiimides such as N, N'-diethyl, N, N ', - dipropyl, N, N'-diisopropyl, N, N'-dicyclohexylcarbodiimide, N- (3-dimethylaminoisopropyl) -N '-ethylcarbodiimide hydrochloride (EDC), N-cyclohexylcarbodiimide-N'-propyloxymethyl-polystyrene (PS-carbodiimide) or carbonyl compounds such as carbonyldiimida zole, or 1,2-oxazolium compounds such as 2-ethyl-5-phenyl-1,2-oxazolium 3-sulphate or 2-tert-butyl-5-methylisoxazolium perchlorate, or acylamino compounds such as 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline, or propanephosphonic anhydride, or isobutylchloroformate, or bis (2-oxo) 3-oxazolidinyl) -phosphoryl chloride or benzotriazolyloxy-tri (dimethylamino) phosphonium hexafluorophosphate, or O- (benzotriazol-1-yl) -N, N, N ', N'-tetra-methyluronium hexafluorophosphate (HBTU), 2- (2-oxo -1- (2H) -pyridyl) -1,1,3,3-tetramethyluronium tetrafluoroborate (TPTU) or O- (7-azabenzotriazol-1-yl) -N, N, N ', N'-tetramethyl-uronium hexafluorophosphate (HATU ), or 1 Hydroxybenzotriazole (HOBt), or benzotriazol-1-yloxytris (dimethylamino) phosphonium hexafluorophosphate (BOP), or N-hydroxysuccinimide, or mixtures of these, with bases.

bases For example, alkali metal carbonates, e.g. Sodium or potassium carbonate, or bicarbonate, or organic bases such as trialkylamines e.g. Triethylamine, N-methylmorpholine, N-methylpiperidine, 4-dimethylaminopyridine or diisopropylethylamine.

Preferably Condensation with HATU or with EDC in the presence of HOBt carried out.

The Compounds of formulas (X) and (XI) are known or can be by known methods from the corresponding starting compounds synthesize.

in welcher R⁹ und R¹⁰ die oben angegebene Bedeutung haben, und
R²⁰ für Methyl oder Ethyl steht.In an alternative method, the compounds of formula (IIc) can be prepared as described in the alternative method for compounds of formula (IIb). Starting compounds are compounds of the formula

in which R ⁹ and R ^{10 have} the abovementioned meaning, and
R ²⁰ is methyl or ethyl.

The Compounds of the formula (XII) are known or can be obtained known methods from the corresponding starting compounds synthesize.

The Preparation of the compounds of the invention can be illustrated by the following synthesis schemes:

Scheme 1

Scheme 2

The Compounds of the invention show an unpredictable, valuable pharmacological activity spectrum.

she are therefore suitable for use as a medicament for treatment and / or prophylaxis of diseases in humans and animals.

at the compounds of the invention are selective inhibitors of the blood coagulation factor Xa, which act in particular as anticoagulants.

Furthermore feature the compounds of the invention on favorable physicochemical Properties such as good solubility in water and physiological Media, what for their therapeutic application is beneficial.

Another The present invention is the use of the compounds of the invention for the treatment and / or prophylaxis of diseases, preferably of thromboembolic disorders and / or thromboembolic Complications.

To the "thromboembolic Diseases "im Senses of the present invention include in particular diseases such as heart attack with ST segment elevation (STEMI) and without ST segment elevation (non-STEMI), stable angina pectoris, unstable angina pectoris, reocclusions and restenosis following coronary interventions such as angioplasty or aortocoronary bypass, peripheral arterial occlusive diseases, pulmonary embolism, deep venous Thrombosis and renal vein thrombosis, transient ischemic attacks as well as thrombotic and thromboembolic stroke.

The Substances are therefore also suitable for the prevention and treatment of Cardiogenic thromboembolism, such as brain ischemia, stroke and systemic thromboembolism and ischaemia, in patients with acute, intermittent or persistent cardiac arrhythmias, such as Atrial fibrillation, and those undergoing cardioversion, also in patients with valvular diseases or with artificial Heart valves. About that In addition, the compounds of the invention suitable for the treatment of disseminated intravascular coagulation (DIC).

thromboembolic Complications also occur in microangiopathic hemolytic anemias, extracorporeal blood circuits, like hemodialysis, and heart valve prostheses.

In addition, the compounds according to the invention are also suitable for the prophylaxis and / or treatment of atherosclerotic vascular diseases and inflammatory diseases such as rheumatic diseases of the musculoskeletal system, moreover also for the prophylaxis and / or treatment of Alzheimer's disease. In addition, the compounds according to the invention can inhibit tumor growth and metastasis, in microangiopathies, age-related macular degeneration, diabetic retinopathy, diabetic nephropathy and other microvascular diseases and for the prevention and treatment of thromboembolic complications, such as venous thromboembolism, in tumor patients, particularly those undergoing major surgery or chemo- or radiotherapy.

The Compounds of the invention can about that also used to prevent coagulation ex vivo be, e.g. for the preservation of blood and plasma products, for Cleaning / pretreatment of catheters and other medical Aids and devices, for coating artificial surfaces of in vivo or ex vivo used medical aids and devices or in biological samples containing factor Xa.

Another The present invention is the use of the compounds of the invention for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases.

Another The present invention is the use of the compounds of the invention for the manufacture of a medicament for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases.

Another The subject of the present invention is a method of treatment and / or prophylaxis of diseases, in particular those mentioned above Diseases using an anticoagulant Amount of the compound of the invention.

Another The present invention is a method for preventing the blood coagulation in vitro, especially in blood or biological samples containing factor Xa characterized is that an anticoagulatory effective amount of the compound of the invention is added.

• • Lipidsenker, insbesondere HMG-CoA-(3-Hydroxy-3-methylglutaryl-Coenzym A)-Reduktase-Inhibitoren;
• • Koronartherapeutika/Vasodilatatoren, insbesondere ACE-(Angiotensin-Converting-Enzyme)-Inhibitoren; AII-(Angiotensin II)-Rezeptor-Antagonisten; β-Adrenozeptor-Antagonisten; alpha-1-Adrenozeptor-Antagonisten; Diuretika; Calciumkanal-Blocker; Substanzen, die eine Erhöhung von cyclischem Guanosinmonophosphat (cGMP) bewirken, wie beispielsweise Stimulatoren der löslichen Guanylatcyclase;
• • Plasminogen-Aktivatoren (Thrombolytika/Fibrinolytika) und die Thrombolysel/Fibrinolyse steigernde Verbindungen wie Inhibitoren des Plasminogen-Aktivator-Inhibitors (PAI-Inhibitoren) oder Inhibitoren des Thrombin-aktivierten Fibrinolyse-Inhibitors (TAFI-Inhibitoren);
• • antikoagulato risch wirksame Substanzen (Antikoagulantien);
• • plättchenaggregationshemmende Substanzen (Plättchenaggregationshemmer, Thrombozytenaggregationshemmer);
• • Fibrinogen-Rezeptor-Antagonisten (Glycoprotein-IIb/IIIa-Antagonisten);
• • sowie Antiarrhythmika.

Another object of the present invention are pharmaceutical compositions containing a compound of the invention and one or more other active ingredients, in particular for the treatment and / or prophylaxis of the aforementioned diseases. As suitable combination active ingredients may be mentioned by way of example and preferably:

• • lipid-lowering drugs, in particular HMG-CoA (3-hydroxy-3-methylglutaryl-coenzyme A) reductase inhibitors;
• Coronary / vasodilators, especially angiotensin converting enzyme (ACE) inhibitors; AII (angiotensin II) receptor antagonists; β-adrenoceptor antagonists; alpha-1-adrenoceptor antagonists; diuretics; Calcium channel blockers; Substances that cause an increase in cyclic guanosine monophosphate (cGMP), such as soluble guanylate cyclase stimulators;
• Plasminogen activators (thrombolytics / fibrinolytics) and thrombolysel / fibrinolysis enhancing compounds such as inhibitors of plasminogen activator inhibitor (PAI inhibitors) or inhibitors of thrombin-activated fibrinolysis inhibitor (TAFI inhibitors);
• • anticoagulant substances (anticoagulants);
• • platelet aggregation inhibiting substances (platelet aggregation inhibitors, antiplatelet agents);
• Fibrinogen receptor antagonists (glycoprotein IIb / IIIa antagonists);
• • as well as antiarrhythmic drugs.

Another The present invention relates to medicaments which are at least a compound of the invention, usually together with one or more inert, non-toxic, pharmaceutical contain suitable excipients, as well as their use to the previously mentioned purposes.

The Compounds of the invention can act systemically and / or locally. For this purpose they can be applied in a suitable manner, e.g. oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, dermal, transdermal, conjunctival, otic or as an implant or stent.

For this Application routes can the compounds of the invention be administered in suitable administration forms.

For the oral administration are according to the prior art functioning, the compounds of the invention rapidly and / or modified donating application forms containing the compounds of the invention in crystalline and / or amorphized and / or dissolved form, such as tablets (non-coated or coated tablets, for example with enteric or delayed-dissolving or insoluble coatings which control the release of the compound of the invention), orally disintegrating tablets or films / wafers, films / lyophilisates, capsules (for example hard or soft gelatin capsules ), Dragees, granules, pellets, powders, emulsions, suspensions, aerosols or solutions.

The Parenteral administration can bypass a resorption step happen (e.g., intravenously, intraarterial, intracardiac, intraspinal or intralumbar) or involving absorption (e.g., intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal). For parenteral administration are suitable as application forms u.a. Injection and infusion preparations in the form of solutions, Suspensions, emulsions, lyophilisates or sterile powders.

For the others Application routes are suitable, e.g. Inhalation medicines (i.a. Powder inhalers, nebulizers), nasal drops, solutions or sprays, lingual, sublingual or buccal tablets to be applied, films / wafers or capsules, suppositories, ear or eye preparations, vaginal capsules, aqueous Suspensions (lotions, shake mixtures), lipophilic suspensions, ointments, creams, transdermal therapeutic Systems (e.g., plasters), milk, pastes, foams, powdered powders, implants or stents.

Prefers are the oral or parenteral administration, especially oral Application.

The Compounds of the invention can in the cited Application forms are transferred. This can be done in a conventional manner by mixing with inert, Non-toxic, pharmaceutically suitable excipients happen. Among these adjuvants include et al excipients (for example, microcrystalline cellulose, lactose, mannitol), solvent (e.g., liquid Polyethylene glycols), emulsifiers and dispersing or wetting agents (For example, sodium dodecyl sulfate, Polyoxysorbitanoleat), binder (For example, polyvinylpyrrolidone), synthetic and natural polymers (for example, albumin), stabilizers (e.g., antioxidants such as for example ascorbic acid), Dyes (e.g., inorganic pigments such as iron oxides) and flavor and / or scent remedies.

in the In general, it has proven to be beneficial in parenteral Application amounts of about 0.001 to 1 mg / kg, preferably about 0.01 to 0.5 mg / kg body weight to achieve effective results. For oral administration is the dosage about 0.01 to 100 mg / kg, preferably about 0.01 to 20 mg / kg and most preferably 0.1 to 10 mg / kg of body weight.

Nevertheless it may be necessary, if necessary, of the quantities mentioned to deviate, depending on of body weight, Route of administration, individual behavior towards the active substance, type of Preparation and time or interval to which the application he follows. So it can in some cases be sufficient, with less than the aforementioned minimum quantity to get along while in other cases exceeded the mentioned upper limit must become. In case of application of larger quantities it may be recommended be to distribute these in several single doses throughout the day.

The following embodiments explain The invention. The invention is not limited to the examples.

The Percentages in the following tests and examples are provided not stated otherwise, weight percentages; Parts are parts by weight. Solvent ratios, dilution ratios and concentration data of liquid / liquid solutions each on the volume.

A. Examples

Abbreviations

• DC

  Thin Layer Chromatography

  DCI

  direct chemical Ionization (in MS)

  DMF

  N, N-dimethylformamide

  DMSO

  dimethyl sulfoxide

  d

  Day (s)

  d. Th.

  the theory (at yield)

  ee

  enantiomeric excess

  eq.

  Equivalent (s)

  IT I

  Electrospray ionization (in MS)

  H

  Hour (s)

  HPLC

  High pressure, high performance liquid chromatography

  LC-MS

  Liquid chromatography-coupled mass spectroscopy

  min

  Minute (s)

  MS

  mass spectroscopy

  NMR

  Nuclear Magnetic Resonance Spectroscopy

  RP

  reverse phase (at HPLC)

  RT

  room temperature

  R _t

  Retention time (at HPLC)

  TBTU

  O- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium tetrafluoroborate

  THF

  tetrahydrofuran

LC-MS and HPLC methods

• Method 1: Device Type MS: Micromass ZQ; device type HPLC: Waters Alliance 2795; Pillar: Phenomenex Synergi 2 μ Hydro-RP Mercury 20 mm × 4 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 210 nm.
• Method 2: Device Type MS: Micromass ZQ; device type HPLC: HP 1100 Series; UV DAD; Pillar: Phenomenex Synergi 2 μ Hydro-RP Mercury 20 mm × 4 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 210 nm.
• Method 3: Instrument: Micromass Quattro LCZ with HPLC Agilent Series 1100; Pillar: Phenomenex Synergi 2 μ Hydro-RP Mercury 20 mm × 4 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 208-400 nm.
• Method 4: Instrument: Micromass Platform LCZ with HPLC Agilent Series 1100; Pillar: Phenomenex Synergi 2 μ Hydro-RP Mercury 20 mm × 4 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 210 nm.
• Method 5: Instrument: Micromass Platform LCZ with HPLC Agilent Series 1100; Pillar: Thermo HyPURITY Aquastar 3 μ 50 now × 2.1 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 liter of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 100% A → 0.2 min 100% A → 2.9 min 30% A → 3.1 min 10% A → 5.5 min 10% A; Oven: 50 ° C; Flow: 0.8 ml / min; UV detection: 210 nm.
• Method 6: Device Type MS: Micromass ZQ; device type HPLC: Waters Alliance 2795; Pillar: Merck Chromolith SpeedROD RP-18e 50 mm × 4.6 mm; Eluent A: 1 liter of water + 0.5 ml of 50% formic acid, Eluent B: 1 liter acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min 10% B → 3.0 min 95% B → 4.0 min 95% B; Oven: 35 ° C; Flow: 0.0 min 1.0 ml / min → 3.0 min 3.0 ml / min → 4.0 min 3.0 ml / min; UV detection: 210 nm.
• Method 7: Device Type MS: Micromass ZQ; device type HPLC: HP 1100 Series; UV DAD; Pillar: Phenomenex Gemini 3 μ 30 mm × 3.00 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 liter acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min. 2 ml / min; Oven: 50 ° C; UV detection: 210 nm.
• Method 8: Instrument: Micromass Quattro LCZ with HPLC Agilent Series 1100; Pillar: Phenomenex Gemini 3 μ 30 mm × 3.00 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 liter acetonitrile + 0.5 ml 50% formic acid; Gradient: 0.0 min 90% A → 2.5 min 30% A → 3.0 min 5% A → 4.5 min 5% A; Flow: 0.0 min 1 ml / min, 2.5 min / 3.0 min / 4.5 min 2 ml / min; Oven: 50 ° C; UV detection: 208-400 nm.
• Method 9: Instrument: HP 1100 with DAD Detection; Column: Kromasil 100 RP-18, 60 mm × 2.1 mm, 3.5 μm; eluent A: 5 ml perchloric acid (70%) / l water, eluent B: acetonitrile; Gradient: 0 min 2% B → 0.5 min 2% B → 4.5 min 90% B → 9 min 0% B → 9.2 min 2% B → 10 min 2% B; Flow: 0.75 ml / min; Column temperature: 30 ° C; UV detection: 210 nm.
• Method 10: Instrument: HP 1100 with DAD Detection; Column: Kromasil 100 RP-18, 60 mm × 2.1 mm, 3.5 μm; eluent A: 5 ml perchloric acid (70%) / l water, eluent B: acetonitrile; Gradient: 0 min 2% B → 0.5 min 2% B → 4.5 min 90% B → 15 min 90% B → 15.2 min 2% B → 16 min 2% B; Flow: 0.75 ml / min; Column temperature: 30 ° C; UV detection: 210 nm.
• Method 11: Instrument: HP 1100 with DAD Detection; Column: Kromasil 100 RP-18, 60 mm × 2.1 mm, 3.5 μm; eluent A: 5 ml perchloric acid (70%) / l water, eluent B: acetonitrile; Gradient: 0 min 2% B → 0.5 min 2% B → 4.5 min 90% B → 6.5 min 90% B → 6.7 min 2% B → 7.5 min 2% B; Flow: 0.75 ml / min; Column temperature: 30 ° C; UV detection: 210 nm.
• Method 12: Instrument: HP 1100 with DAD Detection; Column: Kromasil C18 60 * 2; Eluent A: 0.01 M phosphorus acid, eluent B: acetonitrile, gradient: 0 min 90% A → 0.5 min 90% A, → 4.5 min 10% A, → 6.5 min 10% A; Flow: 0.75 ml / min; Column temperature: 30 ° C; UV detection: 210 nm.
• Method 13: Instrument: Micromass GCT, GC6890; Column: Restek RTX-35, 15 m × 200 μm × 0.33 μm; constant Flow with helium: 0.88 ml / min; Oven: 70 ° C; Inlet: 250 ° C; Gradient: 70 ° C, 30 ° C / min → 310 ° C (3 min hold).

Starting Compounds Example 1A 4-Amino-2-benzofuran-1,3-dione

The Representation of the title compound is analogous to a literature known Method [E.L. Eliel et al., J. Am. Chem. Soc. 1955, 77, 5092-5094].

Example 2A 4-Amino-1H-isoindole-1,3 (2H) -dione

The Representation of the title compound is analogous to a literature known Method [H.D.K. Drew, F.H. Pearman, J. Chem. Soc. 1937, 26-33].

Example 3A 5-Chloro-N- (1,3-dioxo-1,3-dihydro-2-benzofuran-4-yl) thiophene-2-carboxamide

The Preparation of the title compound is carried out analogously to that in WO 03/007942 described method (Example 1).

Example 4A 5-Chloro-N- (1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide

The Representation of the title compound is analogous to that in WO 03/011858 described method (Example 1).

Example 5A 5-Chloro-N- [2- (4-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A suspension of 2.1 g (6.9 mmol) of 5-chloro-N- (1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide (Example 4A) in 20 ml of tetrahydrofuran under argon at RT with a solution of 2.1 g (9.0 mmol, 1.3 eq.) (4-iodophenyl) methanol in 10 ml of tetrahydrofuran and with a solution of 2.3 g (9.0 mmol, 1.3 eq.) Triphenylphosphine in 10 ml of tetrahydrofuran. The reaction suspension is cooled to 0 ° C., admixed with a solution of 1.4 ml (9.0 mmol, 1.3 eq.) Of diethyl azodicarboxylate in 10 ml of tetrahydrofuran (the suspension is converted into a solution) and stirred at RT for 1 h. The reaction mixture is concentrated in vacuo and the residue is stirred with dichloromethane / water.
Yield: 2.5 g (70% purity, 49% of theory)
LC-MS (Method 1): R _t = 3.22 min;
MS (ESIpos): m / z = 521 [M + H] ⁺ .

Example 6A and Example 7A 5-Chloro-N- [2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 6A) and Chloro-N- [2- (4-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 7A)

Step a): Isomer mixture of 5-chloro-N- [1-hydroxy-2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide and 5 -chloro-N- [3-hydroxy-2- (4-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A solution from 2.3 g (70% pure, 3.0 mmol) of 5-chloro-N- [2- (4-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2 carboxamide (Example 5A) in a mixture of 6 ml of methanol and 60 ml of dichloromethane is under argon at 0 ° C with 247 mg (6.5 mmol, 2.2 eq.) of sodium borohydride. The reaction mixture is stirred for 1.5 h at RT and with hydrochloric acid (1N) adjusted to pH 5. The resulting precipitate is filtered, washed with water and dichloromethane and dried in vacuo.

Isomer 1:

• Yield: 1.5 g (88% purity, 57% of theory)
• LC-MS (Method 1): R _t = 2.93 min;
• MS (ESIpos): m / z = 525 [M + H] ⁺ .

To Addition of dichloromethane / water and phase separation becomes the aqueous phase extracted with dichloromethane. The combined, organic phases be over Dried sodium sulfate, filtered and concentrated in vacuo.

isomers:

• Yield: 0.65 g (58% purity, 17% of theory)
• LC-MS (Method 1): R _t = 2.47 min (isomer 2) and 2.93 min (isomer 1);
• MS (ESIpos): m / z = 525 [M + H] ⁺ .

Step b.1): 5-Chloro-N- [2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A Suspension of 1.5 g (88% purity, 2.6 mmol) of 5-chloro-N [1-hydroxy-2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene 2-carboxamide in 20 ml of dichloromethane is added dropwise under argon at RT with 2.7 ml (35.0 mmol, 13 eq.) Of trifluoroacetic acid and 0.93 ml (5.8 mmol, 2.2 eq.) Triethylsilane added. The reaction mixture is at 1 h RT stirred and with saturated, aqueous Sodium bicarbonate solution added. After addition of dichloromethane and phase separation is the watery Phase extracted several times with dichloromethane. The united, organic Phases are over Dried sodium sulfate, filtered and concentrated in vacuo.

Example 6A:

• Yield: 1.4 g (95% of theory)
• LC-MS (Method 3): R _t = 3.32 min; MS (ESIpos): m / z = 509 [M + H] ⁺ ;
• ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 11.27 (s, 1H), 8.25 (d, 1H), 7.72 (d, 2H), 7.64 (d, 1H), 7.59 (t, 1H) , 7.33 (d, 1H), 7.28 (d, 1H), 7.13 (d, 2H), 4.71 (s, 2H), 4.43 (s, 2H).

Stage b.2): 5-Chloro-N- [2- (4-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A Suspension of 0.75 g (58% purity, 0.83 mmol) mixture of isomers in 10 ml of dichloromethane is added dropwise under argon at RT with 1.3 ml (17.0 mmol, 20 eq.) Of trifluoroacetic acid and 0.46 ml (2.9 mmol, 3.5 eq.) Triethylsilane added. The reaction mixture is at 1 h RT stirred and with saturated, aqueous Sodium bicarbonate solution added. After addition of dichloromethane and phase separation is the watery Phase extracted several times with dichloromethane. The united, organic Phases are over Dried sodium sulfate, filtered and concentrated in vacuo. The Title compound is by stirring of the crude product with dichloromethane / methanol isolated.

Example 7A:

• Yield: 149 mg (84% purity, 30% of theory)
• LC-MS (Method 2): R _t = 2.83 min;
• MS (ESIpos): m / z = 509 [M + H] ⁺ .

Example 8A 5-Chloro-N- [2- (3-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A solution of 3.6 g (11.8 mmol) of 5-chloro-N- (1,3-dioxo-1,3-dihydro-2-benzofuran-4-yl) thiophene-2-carboxamide (Example 3A) and 2.7 g (11.8 mmol, 1 eq.). 1 (3-iodophenyl) methanamine in 50 ml of dioxane is treated at RT with 10.3 ml (59.0 mmol, 5 eq.) of N, N-diisopropylethylamine. The reaction mixture is stirred for 9 h under reflux and cooled in an ice bath. The resulting precipitate is filtered, washed with dioxane and dried in vacuo. The combined mother liquors are concentrated in vacuo. The residue is stirred with acetone and the precipitate is filtered, washed with acetone and dried in vacuo.
Yield: 3.9 g (62% of theory)
LC-MS (Method 3): R _t = 3.36 min;
MS (ESIpos): m / z = 523 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.40 (s, 1H), 8.33 (d, 1H), 7.87 (t, 1H), 7.80 (d, 1H), 7.72 (s, 1H) , 7.67 (2 × d, 2H), 7.3 7 (d, 1H), 7.34 (d, 1H), 7.15 (t, 1H), 4.73 (s, 2H).

Example 9A 7-Amino-2- (3-iodobenzyl) isoindolin-1-one

Stage a): 2- (bromomethyl) -6-nitrobenzoic acid methyl ester

A solution of 15.33 g (78.54 mmol) of methyl 2-methyl-6-nitrobenzoate in 300 ml of carbon tetrachloride is charged with 13.98 g (78.54 mmol) of N-bromosuccinimide (NBS) and 129 mg (0.79 mmol) of 2,2'-azobis-2-one. methylpropanenitrile (AIBN) and heated to reflux. After 15 h and after a further 24 h reaction time, in each case an additional 13.98 g (78.54 mmol) of NBS are added. After a total of 111 h reaction time, the reaction mixture is allowed to cool to RT, filtered from the insoluble and removed the solvent on a rotary evaporator. The residue is purified by flash chromatography (silica gel, cyclohexane / dichloromethane 2: 1). Two fractions are obtained. The first consists of 7.7 g (28% yield) of 2- (dibromomethyl) -6-nitrobenzoic acid methyl ester and the second of 12.82 g (60% yield) of the title compound.
GC / MS (Method 13): R _t = 6.58 min;
MS (TOF, EI): m / z = 273/275 ( ⁷⁹ Br / ⁸¹ Br, M ⁺ );
¹ H-NMR (500 MHz, CDCl _3): δ = 8:08 (d, 1H), 7.77 (d, 1H), 7:59 (dd, 1H), 4:58 (s, 2H), 3.99 (s, 3H).

Stage b): 2- (3-iodobenzyl) -7-nitroisoindolin-1-one

A solution of 615 mg (2.24 mmol) of 2- (bromomethyl) -6-nitrobenzoic acid methyl ester in 5 ml of N, N-dimethylformamide is added successively with 549 mg (2.36 mmol) of 1- (3-iodophenyl) methanamine and 630 μl (4.49 mmol). Triethylamine added. After 15 h stirring at 80 ° C is added with about 25 ml of water and extracted three times with dichloromethane. The combined organic extracts are washed successively with water and saturated brine. After drying over anhydrous sodium sulfate is filtered and the filtrate is freed from the solvent in vacuo. The residue obtained is purified by suction filtration through silica gel with dichloromethane / methanol 100: 0 → 100: 1 as eluent. There are 0.83 g (84% yield, based on 90% purity) of the title compound.
HPLC (Method 8): R _t = 2.79 min;
MS (ESIpos): m / z = 395 (M + H) ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 7.91 (d, 1H), 7.87 (d, 1H), 7.81 (dd, 1H), 7.70 (d, 1H), 7.67 (dd, 1H) , 7.32 (d, 1H), 7.18 (dd, 1H), 4.68 (s, 2H), 4.50 (s, 2H).

Step c): 7-Amino-2- (3-iodobenzyl) -isoindolin-1-one

A solution of 830 mg (2.11 mmol) of 2- (3-iodobenzyl) -7-nitroisoindolin-1-one in 15 ml of ethanol is treated with 2.38 g (10.53 mmol) of tin (II) chloride dihydrate and heated to 70 for 75 min ° C heated. Then the reaction mixture is poured into ice-water, brought to pH 8 with saturated sodium bicarbonate solution and filtered through Celite. It is washed with ethyl acetate, the phases are separated and the aqueous phase is evaporated to dryness. The residue of the aqueous phase is combined with the celite filter material and stirred with hot ethanol. After filtration, the ethanol is removed on a rotary evaporator. There remain 671 mg (87% yield) of the title compound, which is reacted further without further purification.
HPLC (Method 7): R _t = 2.71 min;
MS (ESIpos): m / z = 365 (M + H) ⁺ .

Example 10A 5-Chloro-N- [2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

Method 1: Preparation from 5-chloro-N- [2- (3-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 8A) Step a): 5-Chloro N- [1-hydroxy-2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A solution of 3.7 g (7.0 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide ( Example 8A) in a mixture of 8 ml of methanol and 80 ml of dichloromethane under argon at 0 ° C with 398 mg (10.5 mmol, 1.5 eq.) Of sodium borohydride. The reaction mixture is stirred for 1 h at RT and adjusted to pH 5 with hydrochloric acid (1 N). The resulting precipitate is filtered, washed with water and dichloromethane and dried in vacuo.
Yield: 2.3 g (61% of theory)
LC-MS (Method 3): R _t = 3.10 min;
MS (ESIpos): m / z = 525 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.00 (s, 1H), 8.30 (d, 1H), 7.74 (s, 1H), 7.69-7.61 (m, 3H), 7.37 (d, 1H), 7.35-7.30 (m, 2H), 7.15 (t, 1H), 7.00 (d, 1H), 5.80 (d, 1H), 4.80 (d, 1H), 4.43 (d, 1H).

Step b): 5-Chloro-N- [2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A suspension of 2.3 g (4.3 mmol) of 5-chloro-N- [1-hydroxy-2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2 carboxamide in 30 ml of dichloromethane is added dropwise under argon at RT with 4.0 ml (51.5 mmol, 12 eq.) of trifluoroacetic acid and 1.4 ml (8.6 mmol, 2 eq.) of triethylsilane. The reaction mixture is stirred for 20 h at RT and treated with saturated aqueous sodium bicarbonate solution. After addition of dichloromethane and phase separation, the aqueous phase is extracted several times with dichloromethane. The combined organic phases are washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo.
Yield: 1.5 g (97% of theory)
LC-MS (Method 3): R _t = 3.33 min;
MS (ESIpos): m / z = 509 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.23 (s, 1H), 8.27 (d, 1H), 7.71 (s, 1H), 7.68 (d, 1H), 7.65 (d, 1H) , 7.61 (t, 1H), 7.33 (d, 2H), 7.29 (d, 1H), 7.19 (t, 1H), 4.73 (s, 2H), 4.46 (s, 2H).

Method 2: Preparation of 7-amino-2- (3-iodobenzyl) isoindolin-1-one (Example 9A)

A solution of 767 mg (2.11 mmol) of 7-amino-2- (3-iodobenzyl) isoindolin-1-one (Example 9A) in 20 ml of anhydrous dichloromethane is treated with 352 μl (2.53 mmol) of triethylamine and a solution of 419 mg ( 2.32 mmol) of 5-chlorothiophenecarboxylic acid chloride. The reaction mixture is stirred at RT for 15 h. It is then diluted with further dichloromethane and washed successively with water and saturated sodium chloride solution. After drying over anhydrous sodium sulfate is filtered and the filtrate is freed from the solvent in vacuo. The residue obtained is purified by suction filtration through silica gel with cyclohexane / ethyl acetate 5: 1 as eluent. There are obtained 538 mg (50% yield) of the title compound.
HPLC (Method 1): R _t = 3.18 min;
MS (ESIpos): m / z = 509/511 ( ³⁵ Cl / ³⁷ Cl, M + H) ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.25 (s, 1H), 8.26 (d, 1H), 7.71 (s, 1H), 7.68 (d, 1H), 7.66 (d, 1H) , 7.61 (dd, 1H), 7.33 (d, 1H), 7.32 (d, 11H), 7.29 (d, 1H), 7.18 (dd, 1H), 4.73 (s, 2H), 4.47 (s, 2H) ,

Example 11A 4-Amino-2- (3-iodobenzyl) isoindolin-1-one

Stage a): 2- (bromomethyl) -3-nitrobenzoic acid methyl ester

A solution of 21 g (109 mmol) of methyl 2-methyl-3-nitrobenzoate in 300 ml of carbon tetrachloride is stirred under reflux, with 23 g (130 mmol, 1.2 eq.) Of N-bromosuccinimide and 1.8 g (11 mmol, 0.1 eq.). Added 2,2'-azobis-2-methylpropanenitrile and stirred overnight at reflux. After cooling to RT, the reaction mixture is diluted with dichloromethane, washed several times with water, dried over sodium sulfate, filtered and concentrated in vacuo.
Yield: 31 g (quantitative)
HPLC (Method 12): R _t = 4.33 min;
MS (ESIpos): m / z = 273 [M + H] ⁺ ;
¹ H-NMR (300 MHz, DMSO-d ₆ ): δ = 8.16 (d, 1H), 8.11 (d, 1H), 7.74 (t, 1H), 5.03 (s, 2H), 3.92 (s, 3H) ,

Step b): 2- (3-iodobenzyl) -4-nitroisoindolin-1-one

A solution of 2.3 g (8.2 mmol) of 2- (bromomethyl) -3-nitrobenzoate and 1.9 g (8.2 mmol, 1 eq.) Of 1- (3-iodophenyl) methanamine in 40 ml of methanol at RT with 1.3 ml (9.1 mmol , 1.1 eq.) Triethylamine. The reaction mixture is stirred for 3 h at reflux. After cooling to RT, the reaction mixture is mixed with saturated, aqueous ammonium chloride solution. After addition of dichloromethane and phase separation, the aqueous phase is extracted several times with dichloromethane. The combined organic phases are dried over magnesium sulfate, filtered and concentrated in vacuo. The title compound is isolated by flash chromatography (silica gel, dichloromethane / cyclohexane 2: 1 → dichloromethane).
Yield: 2.8 g (87% of theory)
LC-MS (Method 1): R _t = 2.29 min;
MS (ESIpos): m / z = 395 [M + H] ⁺ ;
¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 8.43 (d, 1H), 8.18 (d, 1H), 7.82 (t, 1H), 7.73 (s, 1H), 7.68 (d, 1H) , 7.35 (d, 1H), 7.18 (t, 1H), 4.84 (s, 2H), 4.77 (s, 2H).

Step c): 4-Amino-2- (3-iodobenzyl) isoindolin-1-one

A suspension of 2.6 g (6.5 mmol) of 2- (3-iodobenzyl) -4-nitroisoindolin-1-one in 65 ml of ethanol is treated at RT with 7.4 g (32.7 mmol, 5 eq.) Of tin (II) chloride dihydrate and stirred for 2.5 h at 75 ° C oil bath temperature (formation of a solution). After cooling to RT, the reaction mixture is poured into ice-water, adjusted to pH 8 with saturated aqueous sodium bicarbonate solution, filtered through Celite and the filter cake is washed several times with ethyl acetate. After phase separation, the aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate, filtered and concentrated in vacuo. The title compound is used without further purification in the next reaction.
Yield: 2.0 g (93% of theory)
LC-MS (Method 8): R _t = 2.05 min;
MS (ESIpos): m / z = 365 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 7.70-7.62 (m, 2H), 7.26 (d, 1H), 7.22-7.15 (m, 2H), 6.91 (d, 1H), 6.76 ( d, 1H), 5.40 (s, 2H), 4.69 (s, 2H), 4.11 (s, 2H).

Example 12A 5-Chloro-N- [2- (3-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A solution of 130 mg (0.80 mmol) of 5-chlorothiophenecarboxylic acid in 4 ml of dimethylformamide is treated at RT with 335 mg (0.88 mmol, 1.1 eq.) Of O- (7-azabenzotriazol-1-yl) N, N, N ', N' -tetramethyluronium hexafluoro-phosphate (HATU) and 0.28 ml (1.6 mmol, 2 eq.) of N, N-diisopropylethylamine, stirred for 30 min, with 291 mg (0.80 mmol) of 4-amino-2- (3-iodobenzyl) isoindoline 1-one (Example 11A) and stirred overnight at RT. The title compound is isolated by preparative RP-HPLC (CromSil C18, acetonitrile / water gradient).
Yield: 270 mg (66% of theory)
LC-MS (Method 8): R _t = 2.64 min;
MS (ESIpos): m / z = 509 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.39 (s, 1H), 7.85 (d, 1H), 7.70-7.64 (m, 3H), 7.61 (d, 1H), 7.55 (t, 1H), 7.32-7.25 (m, 2H), 7.16 (t, 1H), 4.70 (s, 2H), 4.41 (s, 2H).

Example 13A 5-Chloro-N- [2- (3-iodo-4-methoxybenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A suspension of 1.3 g (4.2 mmol) of 5-chloro-N- (1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide (Example 4A) in 30 ml of tetrahydrofuran under argon at RT with a solution of 1.5 g (5.5 mmol, 1.3 eq.) of (3-iodo-4-methoxyphenyl) methanol in 10 ml of tetrahydrofuran and with a solution of 1.4 g (5.5 mmol, 1.3 eq.) of triphenylphosphine in 10 ml of tetrahydrofuran was added. The reaction suspension is cooled to 0 ° C., admixed with a solution of 1.1 ml (5.5 mmol, 1.3 eq.) Of diisopropyl azodicarboxylate in 10 ml of tetrahydrofuran (the suspension is converted into a solution) and stirred at RT for 2 h. The reaction mixture is concentrated in vacuo and the residue is stirred with dichloromethane / water.
Yield: 2.0 g (87% of theory)
LC-MS (Method 7): R _t = 3.18 min;
MS (ESIpos): m / z = 553 [M + H] ⁺ .

Example 14A and Example 15A 5-Chloro-N- [2- (3-iodo-4-methoxybenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 14A ) and 5-chloro-N- [2- (3-iodo-4-methoxybenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 15A)

Step a): 5-Chloro-N- [1-hydroxy-2- (3-iodo-4-methoxybenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Isomer 1) and 5-chloro-N- [3-hydroxy-2- (3-iodo-4-methoxybenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2 carboxamide (isomer 2)

A solution from 1.9 g (3.5 mmol) of 5-chloro-N- [2- (3-iodo-4-methoxybenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2 carboxamide (Example 13A) in a mixture of 10 ml of methanol and 100 ml of dichloromethane is under argon at 0 ° C with 199 mg (5.3 mmol, 1.5 eq.) of sodium borohydride. The reaction mixture will over Stirred overnight at RT and with hydrochloric acid (1 N) adjusted to pH 5. The resulting precipitate is filtered, washed with water and dichloromethane and dried in vacuo (Isomer 1).

To Addition of dichloromethane / water and phase separation becomes the aqueous phase extracted with dichloromethane. The combined, organic phases be over Dried sodium sulfate, filtered and concentrated in vacuo (mixture of isomers, Isomer 1 / isomer 2 = 1: 2).

Isomer 1:

• Yield: 662 mg (34% of theory)
• LC-MS (Method 8): R _t = 2.95 min;
• MS (ESIpos): m / z = 555 [M + H] ⁺ ;
• ¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.02 (s, 1H), 8.29 (d, 1H), 7.77 (s, 1H), 7.68-7.60 (m, 2H), 7.39-7.29 ( m, 3H), 7.01-6.93 (m, 2H), 5.74 (d, 1H), 4.78 (d, 1H), 4.34 (d, 1H), 3.80 (s, 3H).

isomers:

• Yield: 1.2 g (64% of theory)
• LC-MS (Method 8): R _t = 2.54 min (isomer 2) and 2.95 min (isomer 1);
• MS (ESIpos): m / z = 555 [M + H] ⁺ .

Step b.1): 5-Chloro-N- [2- (3-iodo-4-methoxybenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A Suspension of 568 mg (1.0 mmol) of isomer 1 in 20 ml of dichloromethane under argon at RT dropwise with 0.95 ml (12.0 mmol, 12 eq.) trifluoroacetic acid and 0.32 ml (2.0 mmol, 2 eq.) of triethylsilane. The reaction mixture is stirred for 1 h at RT and with saturated, aqueous Sodium bicarbonate solution added. After addition of dichloromethane and phase separation is the watery Phase extracted several times with dichloromethane. The united, organic Phases become saturated, aqueous Sodium chloride solution washed over Dried sodium sulfate, filtered and concentrated in vacuo.

Example 14A:

• Yield: 535 mg (97% of theory)
• LC-MS (Method 7): R _t = 3.41 min;
• MS (ESIpos): m / z = 539 [M + H] ⁺ ;
• ¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.29 (s, 1H), 8.27 (d, 1H), 7.75 (s, 1H), 7.67 (d, 1H), 7.60 (t, 1H) , 7.35 (d, 1H), 7.33 (d, 1H), 7.29 (d, 1H), 7.00 (d, 1H), 4.68 (s, 2H), 4.42 (s, 2H), 3.80 (s, 3H).

Step b.2): 5-Chloro-N- [2- (3-iodo-4-methoxybenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide

A suspension of 1.4 g (2.4 mmol) of isomer mixture in 20 ml of dichloromethane is added dropwise under argon at RT with 2.3 ml (29.3 mmol, 12 eq.) Of trifluoroacetic acid and 0.78 ml (4.9 mmol, 2 eq.) Of triethylsilane. The reaction mixture is stirred for 1 h at RT and treated with saturated aqueous sodium bicarbonate solution. After addition of dichloromethane and phase separation, the aqueous phase is extracted several times with dichloromethane. The combined organic phases are washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. The isomers are separated by preparative RP-HPLC (CromSil C18, acetonitrile / water gradient).
Yield: 665 mg (51% of theory) isomer 1 (Example 14A) and
160 mg (12% of theory) isomer 2 (Example 15A)

Example 15A:

• LC-MS (Method 1): R _t = 2.45 min;
• MS (ESIpos): m / z = 539 [M + H] ⁺ ;
• ¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.38 (s, 1H), 7.86 (d, 1H), 7.70 (s, 1H), 7.65 (d, 1H), 7.61 (d, 1H) , 7.56 (t, 1H), 7.31-7.25 (m, 2H), 6.99 (d, 1H), 4.64 (s, 2H), 4.38 (s, 2H), 3.80 (s, 3H).

Example 16A Morpholine-3-one

The Representation of the title compound is analogous to a literature known Method [J.-M. Lehn, F. Montavon, Helv. Chim. Acta 1976, 59, 1566-1583].

Example 17A 4- (4-Aminophenyl) morpholin-3-one

The Represented by substitution of 4-fluoronitrobenzene with Morpholin-3-one (Example 16A) followed by reduction of 4- (4-nitrophenyl) morpholin-3-one (see WO 01/47919, starting compounds I or II, pp 55-57).

Example 18A 3-Hydroxypiperidin-2-one

The Representation of the title compound is analogous to a literature known Method [I.S. Hutchinson et al., Tetrahedron 2002, 58, 3137-3143].

Example 19A 1- (4-Amino-3-fluorophenyl) -3-hydroxypiperidin-2-one

The title compound is prepared analogously to a method known from the literature [A. Klapers et al., J. Am. Chem. Soc. 2002, 124, 7421-7428] from 2-fluoro-4-iodoaniline and 3-hydroxypiperidin-2-one (Example 18A):
A suspension of 6.45 g (27.2 mmol) of 2-fluoro-4-iodoaniline, 3.92 g (34.0 mmol, 1.25 eq.) Of 3-hydroxypiperidin-2-one, 1.04 g (5.5 mmol, 0.2 eq.) Of copper (I) iodide , 11.56 g (54.5 mmol, 2 eq.) Of potassium phosphate and 1.2 ml (10.9 mmol, 0.4 eq.) Of N, N'-dimethylethylenediamine in 157 ml of dioxane is stirred under argon overnight under reflux. Another 1.04 g (5.5 mmol, 0.2 eq.) Of copper (I) iodide and 0.9 ml (8.2 mmol, 0.3 eq.) Of N, N'-dimethylethylenediamine are added. The reaction mixture is stirred for a further 8 h under reflux, filtered after cooling to RT over a diatomaceous earth layer and the residue washed with a mixture of dichloromethane and methanol (1: 1). The combined filtrates are concentrated in vacuo. The crude product is by means of Purified by flash chromatography (silica gel 60, dichloromethane / methanol 100: 1 → 40: 1).
Yield: 2.57 g (41% of theory)
HPLC (Method 11): R _t = 1.52 min;
MS (DCI, NH _3): m / z = 242 [M + NH _4] ^+;
1 H-NMR (300 MHz, DMSO-d ₆ ): δ = 6.94 (d, 1H), 6.81-6.65 (m, 2H), 5.12 (br, s, 2H), 3.99 (dt, 1H), 3.63- 3.39 (m, 2H), 2.12-2.00 (m, 1H), 2.00-1.62 (m, 4H).

Example 20A 3 - ({[tert-butyl (diphenyl) silyl] oxy} methyl) piperidin-2-one

A solution of 5.0 g (38.7 mmol) of 3-hydroxymethylpiperidin-2-one [J. Yang et al., Org. Lett. 2000, 2, 763-766] in 40 ml of N, N-dimethylformamide is added sequentially with 3.16 g (46.5 mmol) of imidazole and dropwise with 11 ml (42.6 mmol) of tert-butyl (diphenyl) silyl chloride. After 3 h at RT, it is mixed with about 400 ml of water and extracted three times with ethyl acetate. The combined organic extracts are washed successively with saturated ammonium chloride solution, water and saturated brine. After drying over anhydrous magnesium sulfate, it is filtered and the filtrate is freed from the solvent in vacuo. The residue obtained is purified by suction filtration through silica gel with cyclohexane / ethyl acetate 20: 1 → 1: 1 as eluent. There are obtained 9.43 g (66% of theory) of the title compound.
HPLC (Method 1): R _t = 2.79 min;
MS (ESIpos): m / z = 368 (M + H) ⁺ ;
¹ H-NMR (400 MHz, CDCl ₃ ): δ = 7.69-7.65 (m, 4H), 7.42-7.34 (m, 6H), 5.82 (s, broad, 1H), 4.03 (dd, 1H), 3.93 ( dd, 1H), 3.32-3.28 (m, 2H), 2.53-2.48 (m, 1H), 2.07-1.99 (m, 1H), 1.96-1.87 (m, 2H), 1.78-1.68 (m, 1H), 1.04 (s, 9H).

embodiments

General method 1 for the coupling of Aryl iodides with lactams:

A Suspension of copper (I) iodide (0.2 eq.) And potassium phosphate (2 eq.) in dioxane (30 ml / mmol) under argon at RT with the appropriate Aryl iodide (1 eq.), Lactam (1.5 eq.) And N, N'-dimethylethylenediamine (0.4 eq.). The reaction mixture is refluxed touched, after cooling filtered to RT and the residue washed with dioxane. The combined filtrates are in vacuo concentrated. The title compound is purified by preparative RP-HPLC (CromSil C18, acetonitrile / water gradient).

Example 1 5-Chloro-N- {1,3-dioxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2 carboxamide

A solution of 480 mg (1.56 mmol) of 5-chloro-N- (1,3-dioxo-1,3-dihydro-2-benzofuran-4-yl) thiophene-2-carboxamide (Example 3A) and 300 mg (1.56 mmol, 1 eq.) of 4- (4-aminophenyl) morpholin-3-one (example 17A) in 7 ml of dioxane is added at room temperature with 1.1 ml (7.8 mmol, 5 eq.) Of triethylamine. The reaction mixture is stirred for 4 h under reflux and then cooled in an ice bath. The resulting precipitate is filtered, washed with dioxane and dried in vacuo.
Yield: 633 mg (84% of theory)
HPLC (Method 11): R _t = 4.54 min;
MS (ESIpos): m / z = 482 [M + H] ⁺ ;
¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 10.50 (s, 1H), 8.42 (d, 1H), 7.92 (t, 1H), 7.78 (d, 1H), 7.74 (d, 1H) , 7.58 (d, 2H), 7.50 (d, 2H), 7.33 (d, 1H), 4.23 (s, 2H), 4.00 (t, 2H), 3.82 (t, 2H).

Example 2 and Example 3 5-Chloro-N- {3-oxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2 carboxamide (Example 2) and 5-chloro-N- {1-oxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene -2-carboxamide (Example 3)

Step a): Isomer mixture of 5-chloro-N- {1-hydroxy-3-oxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindole-4 yl} thiophene-2-carboxamide and 5-chloro-N- {3-hydroxy-1-oxo-2- [4- (3-oxomorpholin-4-yl) -phenyl] -2,3-dihydro-1H-isoindole- 4-yl} thiophene-2-carboxamide

A solution of 300 mg (0.62 mmol) of 5-chloro-N- {1,3-dioxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindole-4 -yl} thiophene-2-carboxamide (Example 1) in a mixture of 20 ml of methanol and 20 ml of dichloromethane is added under argon at 0 ° C with 35 mg (0.93 mmol, 1.5 eq.) Of sodium borohydride. The reaction mixture is stirred for 2 h at RT and brought to pH 5 with hydrochloric acid (1 N). After addition of dichloromethane and phase separation, the aqueous phase is extracted several times with dichloromethane. The combined organic phases are dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product is used without further purification in the next stage.
Yield: 240 mg (80% of theory)
LC-MS (Method 1): R _t = 1.80 min;
MS (ESIpos): m / z = 483 [M + H] ⁺ .

Step b): 5-Chloro-N- {3-oxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2 carboxamide and 5-chloro-N- {1-oxo-2- [4- (3-oxomorpholin-4-yl) phenyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

A solution of 240 mg (0.5 mmol) of isomer mixture of stage a) in 3 ml of dichloromethane is added Argon at RT added dropwise with 0.23 ml (3.0 mmol, 6 eq.) Trifluoroacetic acid and 79 .mu.l (0.5 mmol, 1 eq.) Of triethylsilane. The reaction mixture is stirred for 2 d at RT and treated with saturated aqueous sodium bicarbonate solution. After addition of dichloromethane and phase separation, the aqueous phase is extracted several times with dichloromethane. The combined organic phases are dried over magnesium sulfate, filtered and concentrated in vacuo. The isomers are isolated by preparative RP-HPLC (CromSil C18, acetonitrile / water gradient).

Example 2 (Isomer 1):

• Yield: 2 mg (2% of theory)
• LC-MS (Method 1): R _t = 2.43 min;
• MS (ESIpos): m / z = 468 [M + H] ⁺ ;
• ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 11.28 (s, 1H), 8.31 (d, 1H), 7.93 (d, 2H), 7.69 (t, 1H), 7.67 (d, 1H) , 7.50 (d, 2H), 7.40 (d, 1H), 7.36 (d, 1H), 5.10 (s, 2H), 4.22 (s, 2H), 4.00 (t, 2H), 3.78 (t, 2H).

Example 3 (Isomer 2):

• Yield: 44 mg (38% of theory)
• HPLC (Method 9): R _t = 4.15 min;
• MS (ESIpos): m / z = 468 [M + H] ⁺ ;
• ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 10.50 (s, 1H), 7.98-7.89 (m, 3H), 7.76 (d, 1H), 7.70 (d, 1H), 7.60 (t, 1H), 7.47 (d, 2H), 7.33 (d, 1H), 5.04 (s, 2H), 4.21 (s, 2H), 3.99 (t, 2H), 3.76 (t, 2H).

Example 4 5-Chloro-N- {3-oxo-2- [4- (3-oxomorpholin-4-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

According to General Method 1, 76 mg (0.15 mmol) of 5-chloro-N- [2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 6A) and 23 mg (0.23 mmol, 1.5 eq.) Of morpholin-3-one (Example 16A).
Yield: 58 mg (53% of theory)
LC-MS (Method 1): R _t = 2.34 now;
MS (ESIpos): m / z = 482 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.27 (s, 1H), 8.24 (d, 1H), 7.63 (d, 1H), 7.58 (t, 1H), 7.35 (m, 4H) , 7.31 (d, 1H), 7.28 (d, 1H), 4.74 (s, 2H), 4.46 (s, 2H), 4.17 (s, 2H), 3.93 (t, 2H), 3.69 (t, 2H).

Example 5 5-Chloro-N- {1-oxo-2- [4- (3-oxomorpholin-4-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

According to General Method 1, 91 mg (84% purity, 0.15 mmol) of 5-chloro-N- [2- (4-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene 2-carboxamide (Example 7A) and 23 mg (0.23 mmol, 1.5 eq.) Of morpholin-3-one (Example 16A).
Yield: 15 mg (14% of theory)
LC-MS (Method 1): R _t = 1.86 min;
MS (ESIpos): m / z = 482 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.39 (s, 1H), 7.87 (d, 1H), 7.67 (d, 1H), 7.63 (d, 1H), 7.55 (t, 1H) , 7.38 (d, 2H), 7.31 (d, 2H), 7.28 (d, 1H), 4.74 (s, 2H), 4.43 (s, 2H), 4.19 (s, 2H), 3.95 (t, 2H), 3.71 (t, 2H).

Example 6 5-Chloro-N- {3-oxo-2- [3- (3-oxomorpholin-4-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

According to General Method 1, 100 mg (0.2 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 10A) and 30 mg (0.3 mmol, 1.5 eq.) Of morpholin-3-one (Example 16A).
Yield: 34 mg (36% of theory)
LC-MS (method 1): R _t = 2.35 min;
MS (ESIpos): m / z = 482 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.29 (s, 1H), 8.28 (d, 1H), 7.67 (d, 1H), 7.60 (t, 1H), 7.42 (t, 1H) , 7.38 (s, 1H), 7.35-7.28 (m, 3H), 7.24 (d, 1H), 4.78 (s, 2H), 4.48 (s, 2H), 4.19 (s, 2H), 3.97 (t, 2H ), 3.73 (t, 2H).

Example 7 5-Chloro-N- {1-oxo-2- [3- (3-oxomorpholin-4-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

According to General Method 1, 76 mg (0.15 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 12A) and 23 mg (0.23 mmol, 1.5 eq.) Of morpholin-3-one (Example 16A).
Yield: 40 mg (37% of theory)
LC-MS (Method 1): R _t = 1.88 min;
MS (ESIpos): m / z = 482 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.40 (s, 1H), 7.85 (d, 1H), 7.67 (d, 1H), 7.61 (d, 1H), 7.55 (t, 1H) , 7.40 (t, 1H), 7.34 (s, 1H), 7.31 (d, 1H), 7.28 (d, 1H), 7.18 (d, 1H), 4.75 (s, 2H), 4.42 (s, 2H), 4.18 (s, 2H), 3.95 (t, 2H), 3.71 (t, 2H).

Example 8 5-Chloro-N- {2- [4-methoxy-3- (3-oxomorpholin-4-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxamide

According to General Method 1, 162 mg (0.3 mmol) of 5-chloro-N- [2- (3-iodo-4-methoxybenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl ] thiophene-2-carboxamide (Example 14A) and 45 mg (0.45 mmol, 1.5 eq.) of morpholin-3-one (Example 16A).
Yield: 83 mg (35% of theory)
LC-MS (Method 7): R _t = 2.61 min;
MS (ESIpos): m / z = 512 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.30 (s, 1H), 8.26 (d, 1H), 7.65 (d, 1H), 7.60 (t, 1H), 7.35 (d, 1H) , 7.30 (t, 2H), 7.20 (s, 1H), 7.11 (d, 1H), 4.70 (s, 2H), 4.42 (s, 2H), 4.15 (s, 2H), 3.92 (t, 2H), 3.79 (s, 3H), 3.52 (t, 2H).

Example 9 5-Chloro-N- {2- [4-methoxy-3- (3-oxomorpholin-4-yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxamide

According to General Method 1, 90 mg (0.17 mmol) of 5-chloro-N- [2- (3-iodo-4-methoxybenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl) thiophene 2-carboxamide (Example 15A) and 25 mg (0.25 mmol, 1.5 eq.) Of morpholin-3-one (Example 16A).
Yield: 13 mg (10% of theory)
LC-MS (Method 8): R _t = 2.05 min;
MS (ESIpos): m / z = 512 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d6): δ = 10.40 (s, 1H), 7.87 (d, 1H), 7.64 (d, 1H), 7.61 (d, 1H), 7.54 (t, 1H), 7.29 (d, 1H), 7.26 (d, 1H), 7.16 (s, 1H), 7.10 (d, 1H), 4.68 (s, 2H), 4.40 (s, 2H), 4.15 (s, 2H), 3.92 (t, 2H), 3.78 (s, 3H), 5.51 (t, 2H).

Example 10 5-Chloro-N- {2- [2-fluoro-4- (3-hydroxy-2-oxopiperidin-1-yl) phenyl] -1,3-dioxo-2,3-dihydro-1H-isoindole 4-yl} thiophene-2-carboxamide

A solution of 412 mg (1.34 mmol) of 5-chloro-N- (1,3-dioxo-1,3-dihydro-2-benzofuran-4-yl) thiophene-2-carboxamide (Example 3A) and 300 mg (1.34 mmol) mmol, 1 eq.). 1- (4-Amino-3-fluorophenyl) -3-hydroxypiperidin-2-one (Example 19A) in 5 ml of dioxane is added at RT with 1.2 ml (6.7 mmol, 5 eq.) N, N -Diisopropylethylamin added. The reaction mixture is stirred overnight under reflux and then cooled in an ice bath. The resulting precipitate is filtered, washed with dioxane and dried in vacuo.
Yield: 459 mg (67% of theory)
LC-MS (Method 3): R _t = 2.61 min;
MS (ESIpos): m / z = 514 [M + H] ⁺ ;
¹ H-NMR (400 MHz, DMSO-d ₆ ): δ = 10.48 (s, 1H), 8.40 (d, 1H), 7.95 (t, 1H), 7.87-7.71 (m, 2H), 7.58 (t, 1H), 7.50 (d, 1H), 7.40-7.27 (m, 2H), 5.49 (s, 1H), 4.12 (m, 1H), 3.85-3.70 (m, 1H), 3.70-3.60 (m, 1H) , 2.20-2.07 (m, 1H), 2.07-1.84 (m, 2H), 1.84-1.70 (m, 1H).

Example 11 5-Chloro-N- {2- [4- (3-hydroxy-2-oxopiperidin-1-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxamide

According to General Method 1, 76 mg (0.15 mmol) of 5-chloro-N- [2- (4-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 6A) and 26 mg (0.23 mmol, 1.5 eq.) Of 3-hydroxypiperidin-2-one (Example 18A).
Yield: 14 mg (12% of theory)
LC-MS (Method 8): R _t = 2.47 min;
MS (ESIpos): m / z = 496 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.29 (s, 1H), 8.26 (d, 1H), 7.66 (d, 1H), 7.60 (t, 1H), 7.38-7.30 (m, 3H), 7.30-7.22 (m, 3H), 5.26 (s, 1H), 4.76 (s, 2H), 4.49 (s, 2H), 4.10-4.00 (m, 1H), 3.70-3.60 (m, 1H) , 3.57-3.47 (m, 1H), 2.13-2.03 (m, 1H), 2.00-1.81 (m, 2H), 1.79-1.68 (m, 1H).

Example 12 5-Chloro-N- {2- [3- (3-hydroxy-2-oxopiperidin-1-yl) benzyl] -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxamide

According to General Method 1, 76 mg (0.15 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2 carboxamide (Example 8A) and 26 mg (0.23 mmol, 1.5 eq.) 3-hydroxypiperidin-2-one (Example 18A).
Yield: 13 mg (11% of theory)
LC-MS (method 1): R _t = 2.40 min;
MS (ESIpos): m / z = 510 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.43 (s, 1H), 8.31 (d, 1H), 7.87 (t, 1H), 7.80 (d, 1H), 7.69 (d, 1H) , 7.40-7.30 (m, 2H), 7.26 (s, 1H), 7.20 (t, 2H), 5.25 (d, 1H), 4.76 (s, 2H), 4.09-4.00 (m, 1H), 3.69-3.60 (m, 1H), 3.55-3.46 (m, 1H), 2.12-2.02 (m, 1H), 1.98-1.80 (m, 2H), 1.79-1.69 (m, 1H).

Example 13 5-Chloro-N- {2- [3- (3-hydroxy-2-oxopiperidin-1-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxamide

According to General Method 1, 100 mg (0.2 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -3-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 10A) and 34 mg (0.3 mmol, 1.5 eq.) Of 3-hydroxypiperidin-2-one (Example 18A).
Yield: 24 mg (16% of theory)
LC-MS (Method 7): R _t = 2.68 min;
MS (ESIpos): m / z = 496 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 11.29 (s, 1H), 8.27 (d, 1H), 7.66 (d, 1H), 7.60 (t, 1H), 7.39 (t, 1H) , 7.34 (d, 1H), 7.30 (d, 1H), 7.25 (s, 1H), 7.21 (t, 2H), 5.23 (d, 1H), 4.77 (s, 2H), 4.47 (s, 2H), 4.08-4.00 (m, 1H), 3.70-3.61 (m, 1H), 3.59-3.50 (m, 1H), 2.12-2.03 (m, 1H), 2.00-1.80 (m, 2H), 1.79-1.69 (m , 1H).

Example 14 5-Chloro- N - {2- [3- (3-hydroxy-2-oxopiperidin-1-yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxamide

According to General Method 1, 76 mg (0.15 mmol) of 5-chloro-N- [2- (3-iodobenzyl) -1-oxo-2,3-dihydro-1H-isoindol-4-yl] thiophene-2-carboxamide (Example 12A) and 26 mg (0.23 mmol, 1.5 eq.) Of 3-hydroxypiperidin-2-one (Example 18A).
Yield: 12 mg (11% of theory)
LC-MS (Method 7): R _t = 2.10 min;
MS (ESIpos): m / z = 496 [M + H] ⁺ ;
¹ H-NMR (500 MHz, DMSO-d ₆ ): δ = 10.40 (s, 1H), 7.87 (d, 1H), 7.67 (d, 1H), 7.63 (d, 1H), 7.56 (t, 1H) , 7.38 (t, 1H), 7.28 (d, 1H), 7.24-7.18 (m, 2H), 7.15 (d, 1H), 5.21 (d, 1H), 4.73 (s, 2H), 4.41 (s, 2H ), 4.08-4.00 (m, 1H), 3.69-3.60 (m 1H), 3.57-3.48 (m, 1H), 2.12-2.02 (m, 1H), 1.98-1.80 (m, 2H), 1.78-1.68 ( m, 1H).

Example 15 5-Chloro-N- {3-oxo-2- [3- (2-oxopiperidin-1-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxylic acid amide

Example 16 5-Chloro-N- {1-oxo-2- [3- (2-oxopiperidin-1-yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxylic acid amide

Example 17 N- (2- {3 - [(3S) -3-amino-2-oxopiperidin-1-yl] benzyl} -3-oxo-2,3-dihydro-1H-isoindol-4-yl) -5 -chlorthiophen-2-carboxylic acid amide

Example 18 N- (2- {3 - [(3S) -3-amino-2-oxopiperidin-1-yl] benzyl} -1-oxo-2,3-dihydro-1H-isoindol-4-yl) -5 -chlorthiophen-2-carboxylic acid amide

Example 19 5-Chloro-N- {2- [3- (3-hydroxy-3-methyl-2-oxopiperidin-1-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindole-4 yl} thiophene-2-carboxamide

Example 20 5-Chloro-N- {2- [3- (3-hydroxy-3-methyl-2-oxopiperidin-1-yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindole-4 yl} thiophene-2-carboxamide

Example 21 5-Chloro-N- (2- {3- [3- (hydroxymethyl) -2-oxopiperidin-1-yl] benzyl} -3-oxo-2,3-dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide

Example 22 5-Chloro-N- (2- {3- [3- (hydroxymethyl) -2-oxopiperidin-1-yl] benzyl} -1-oxo-2,3-dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide

Example 23 5-Chloro- N - (2- {3- [3- (1-hydroxy-1-methylethyl) -2-oxopiperidin-1-yl] benzyl} -3-oxo-2,3-dihydro-1H- isoindol-4-yl) thiophene-2-carboxamide

Example 24 5-Chloro- N - (2- {3- [3- (1-hydroxy-1-methylethyl) -2-oxopiperidin-1-yl] benzyl} -1-oxo-2,3-dihydro-1H- isoindol-4-yl) thiophene-2-carboxamide

Example 25 5-Chloro-N- {2- [3- (3-methyl-2-oxotetrahydropyrimidin-1 (2H) -yl) -benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl } thiophene-2-carboxamide

Example 26 5-Chloro-N- {2- [3- (3-methyl-2-oxotetrahydropyrimidin-1 (2H) -yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindol-4-yl } thiophene-2-carboxamide

Example 27 5-Chloro-N- {2- [3- (3- (2-hydroxyethyl) -2-oxotetrahydropyrimidin-1 (2H) -yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindole -4-yl} thiophene-2-carboxamide

Example 28 5-Chloro-N- {2- [3- (3- (2-hydroxyethyl) -2-oxotetrahydropyrimidin-1 (2H) -yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindole -4-yl} thiophene-2-carboxamide

Example 29 5-Chloro-N- (3-oxo-2- {3- [2-oxo-3- (2-pyrrolidin-1-yl-ethyl) -tetrahydropyrimidin-1 (2H) -yl] -benzyl} -2,3- dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide

Example 30 5-Chloro-N- (1-oxo-2- {3- [2-oxo-3- (2-pyrrolinedin-1-yl-ethyl) -tetrahydropyrimidin-1 (2H) -yl] -benzyl} -2,3 dihydro-1H-isoindol-4-yl) thiophene-2-carboxamide

Example 31 5-Chloro-N- {3-oxo-2- [3- (2-oxopyridin-1 (2H) -yl) -benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2 -carboxamide

Example 32 5-Chloro- N - {1-oxo-2- [3- (2-oxopyridin-1 (2H) -yl) benzyl] -2,3-dihydro-1H-isoindol-4-yl} thiophene-2 -carboxamide

Example 33 5-Chloro-N- (2- {3- [3- (hydroxymethyl) -2-oxopyridine-1 (2H) -yl] -benzyl} -3-oxo-2,3-dihydro-1H-isoindole-4 -yl) thiophene-2-carboxamide

Example 34 5-Chloro-N- (2- {3- [3- (hydroxymethyl) -2-oxopyridine-1 (2H) -yl] -benzyl} -1-oxo-2,3-dihydro-1H-isoindole-4 -yl) thiophene-2-carboxamide

Example 35 5-Chloro-N- (2- {3- [3- (2-hydroxyethoxy) -2-oxopyridine-1 (2H) -yl] -benzyl} -3-oxo-2,3-dihydro-1H-isoindole -4-yl) thiophene-2-carboxamide

Example 36 5-Chloro-N- (2- {3- [3- (2-hydroxyethoxy) -2-oxopyridine-1 (2H) -yl] -benzyl} -1-oxo-2,3-dihydro-1H-isoindole -4-yl) thiophene-2-carboxamide

Example 37 5-Chloro- N - [2- (3- {3 - [(dimethylamino) methyl] -2-oxopyridine-1 (2H) -yl} benzyl) -3-oxo-2,3-dihydro-1H- isoindol-4-yl] thiophene-2-carboxamide

Example 38 5-Chloro-N- [2- (3- {3 - [(dimethylamino) methyl] -2-oxopyridine-1 (2H) -yl} benzyl) -1-oxo-2,3-dihydro-1H- isoindol-4-yl] thiophene-2-carboxamide

Example 39 5-Chloro-N- {2- [3- (1-methyl-2-oxopiperidin-3-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxylic acid amide

Example 40 5-Chloro- N - {2- [3- (1-methyl-2-oxopiperidin-3-yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene 2-carboxylic acid amide

Example 41 5-Chloro-N- {2- [3- (2-hydroxypyridin-3-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxylic acid amide

Example 42 5-Chloro-N- {2- [3- (2-hydroxypyridin-3-yl) benzyl] -1-oxo-2,3-dihydro-1H-isoindol-4-yl} thiophene-2-carboxylic acid amide

Example 43 5-Chloro-N- {2- [3- (1-methyl-2-oxo-1,2-dihydropyridin-3-yl) -benzyl] -3-oxo-2,3-dihydro-1H-isoindole 4-yl} thiophene-2-carboxamide

Example 44 5-Chloro-N- {2- [3- (1-methyl-2-oxo-1,2-dihydropyridin-3-yl) benzyl] -3-oxo-2,3-dihydro-1H-isoindole 4-yl} thiophene-2-carboxamide

B. Evaluation of Pharmacological Activity

The Compounds of the invention In particular, they act as selective inhibitors of the blood coagulation factor Xa and do not inhibit or only at significantly higher concentrations also other serine proteases such as plasmin or trypsin.

"Selective" refers to those coagulation factor Xa inhibitors in which the IC ₅₀ values for factor Xa inhibition are at least 100-fold smaller than the IC ₅₀ values for the inhibition of other serine proteases, in particular plasmin and trypsin , reference being made to the test methods of selectivity for the test methods of examples Ba1) and Ba2) described below.

The advantageous pharmacological properties of the compounds of the invention can through following methods are found:

a) Test descriptions (in vitro)

a.1) Measurement of Factor Xa Inhibition

a.1.1) Chromogenic assay:

The enzymatic activity of human factor Xa (FXa) is measured by the reaction of a FXa-specific chromogenic substrate. The factor Xa cleaves from the chromogenic substrate p-nitroaniline. The determinations are carried out in microtiter plates as follows:
The test substances are dissolved in DMSO at different concentrations and incubated for 10 minutes with human FXa (0.5 nmol / l dissolved in 50 mmol / l Tris buffer [C, C, C-tris (hydroxymethyl) aminomethane], 150 mmol / l NaCl, 0.1% BSA [bovine serum albumine], pH = 8.3) at 25 ° C. The control is pure DMSO. Subsequently, the chromogenic substrate (150 .mu.mol / l Pefachrome ^® FXa from Pentapharm) is added. After 20 minutes incubation at 25 ° C, the absorbance at 405 nm is determined. The extinctions of the test mixtures with test substance are compared with the control batches without test substance and the IC ₅₀ values are calculated therefrom.

Representative Action data from this test are listed in Table 1 below:

Table 1

a.1.2) Fluorogenic assay:

The enzymatic activity of human factor Xa (FXa) is about the implementation of a FXa specific measured fluorogenic substrate. It splits FXa from the peptic Substrate Aminomethylcoumarin, which is measured fluorescently. The determinations are carried out in microtiter plates.

To be tested substances are dissolved in different concentrations in dimethyl sulfoxide and 15 min with human FXa (1.3 nmol / l dissolved in 50 mmol / l Tris buffer [C, C, C-tris (hydroxymethyl) -aminomethan], 100 mmol / l NaCl , 0.1% BSA [bovine serum albumin], pH 7.4) at 22 ° C. Subsequently, the fluorogenic substrate (5 .mu.mol / l Boc-Ile-Glu-Gly-Arg-AMC from Bachem) is added. After incubation for 30 min, the sample is excited at a wavelength of 360 nm and the emission is measured at 460 nm. The measured emissions of the test mixtures with test substance are compared with the test batches without test substance (excluding dimethyl sulfoxide instead of test substance in dimethylsulfoxide) and IC ₅₀ values are calculated from the concentration-activity relationships.

a.2) Determination of selectivity

a.2.1) Chromogenic assay:

To detect selective FXa inhibition, the test substances are tested for their inhibition of other human serine proteases, such as trypsin and plasmin. To determine the enzymatic activity of trypsin (500 mU / ml) and plasmin (3.2 nmol / l), these enzymes are dissolved in Tris buffer (100 mmol / l, 20 mmol / l CaCl ₂ , pH = 8.0) and for 10 minutes incubated with test substance or solvent. Then, by adding the corresponding specific chromogenic substrates (. Chromozym Trypsin ^® and Chromozym Plasmin ^®; Roche Diagnostics company) is started, the enzymatic reaction and the extinction is determined after 20 minutes at 405 nm. All determinations are carried out at 37 ° C. The extinctions of the test mixtures with test substance are compared with the control samples without test substance and from this the IC ₅₀ values are calculated.

a.2.2) Fluorogenic assay:

To demonstrate the selectivity of the substances with respect to factor Xa inhibition, the test substances are tested for their inhibition of other human serine proteases, such as trypsin and plasmin. To determine the enzymatic activity of trypsin (83 mU / ml from Sigma) and plasmin (0.1 μg / ml from Kordia), these enzymes are dissolved (50 mmol / l Tris buffer [C, C, C tris (hydroxymethyl) aminomethane ], 100 mmol / l NaCl, 0.1% BSA [bovine serum albumin], 5 mmol / l calcium chloride, pH 7.4) and incubated for 15 min with test substance in various concentrations in dimethylsulfoxide and with dimethyl sulfoxide without test substance. The enzymatic reaction is then started by addition of the appropriate substrates (5 μmol / L Boc-Ile-Glu-Gly-Arg-AMC from Bachem for trypsin and 50 μmol / l MeOSuc-Ala-Phe-Lys-AMC from Bachem for plasmin). , After an incubation period of 30 min at 22 ° C, the fluorescence is measured (excitation: 360 nm, emission: 460 nm). The measured emissions of the test mixtures with test substance are compared with the test batches without test substance (excluding dimethyl sulfoxide instead of test substance in dimethylsulfoxide) and IC ₅₀ values are calculated from the concentration-activity relationships.

a.3) Determination of anticoagulant effect

The anticoagulant effect of the test substances is determined in vitro in human and rabbit plasma. For this purpose, blood is taken off using a 0.11 molar sodium citrate solution as a template in a sodium citrate / blood mixing ratio of 1: 9. The blood is mixed well immediately after collection and centrifuged for 10 minutes at about 2500 g. The supernatant is pipetted off. The prothrombin time (PT, synonyms: thromboplastin time, quick test) in the presence of varying concentrations of test substance or the corresponding solvent using a commercial test kit determined (Hemoliance ^® RecombiPlastin, from Instrumentation Laboratory.). The test compounds are incubated for 3 minutes at 37 ° C with the plasma. Subsequently, coagulation is triggered by the addition of thromboplastin and the time of coagulation is determined. The concentration of test substance is determined which causes a doubling of the prothrombin time.

b) Determination of the antithrombotic effect (in vivo)

b.1) Arteriovenous shunt model (rabbit)

Sober Rabbits (strain: ESD: NZW) are given by intramuscular administration a Rompun / Ketavet solution anesthetized (5 mg / kg or 40 mg / kg). The thrombus formation is in an arteriovenous Shunt based on that of C.N. Berry et al. [Semin. Thromb. Hemost. 1996, 22, 233-241] triggered method. These are the left vena jugularis and the right carotid artery dissected. An extracorporeal shunt is made by means of a 10 cm long venous catheter placed between the two vessels. This catheter is in the middle in another, 4 cm long Polyethylene tubing (PE 160, Becton Dickenson) used to produce a thrombogenic surface includes a roughened and looped nylon thread incorporated. The extracorporeal circuit is maintained for 15 minutes. Then the shunt is removed and the nylon thread with the thrombus weighed immediately. The empty weight of the nylon thread is before the start of the test been determined. The test substances are administered either intravenously over a prior to application of the extracorporeal circuit Eared vein or orally administered by gavage.

c) solubility assay

needed reagents:

• • PBS buffer pH 7.4: 90.00 g NaCl pa (eg Merck Art. No. 1.06404.1000), 13.61 g KH ₂ PO ₄ pa (eg Merck Art. No. 1.04873.1000) and 83.35 g 1N NaOH (eg Bernd Kraft GmbH Art. No. 01030.4000) into a 1 l volumetric flask, fill up with water and stir for approx. 1 hour.
• • Acetate buffer pH 4.6: Weigh out 5.4 g sodium acetate × 3 H ₂ O pa (eg Merck Art. No. 1.06267.0500) into a 100 ml volumetric flask, dissolve in 50 ml water, add 2.4 g glacial acetic acid, make up to 100 ml with water , check the pH and adjust to pH 4.6 if necessary.
• • dimethyl sulphoxide (e.g., Baker Art. No. 7157,2500)
• • distilled water

Preparation of the calibration solutions:

Preparation of the starting solution for calibration solutions (stock solution: in a 2 ml Eppen village-Safe-Lock Tube (Eppendorf Art. No. 0030 120,094) are weighed approximately 0.5 mg of the drug accurately, to a concentration of 600 ug / ml with DMSO added (eg 0.5 mg of active ingredient + 833 ul DMSO) and to complete Shaken solution by means of a vortexer.

Calibration solution 1 (20 μg / ml): Add 34.4 μl of the stock solution with 1000 μl DMSO mixed and homogenized.

Calibration Solution 2 (2.5 μg / ml): Add 100 μl of Calibration Solution 1 with 700 μl DMSO mixed and homogenized.

Preparation of the sample solutions:

Sample solution for solubility up to 10 g / l in PBS buffer pH 7.4: in a 2 ml Eppendorf Safe-Lock Tube (Eppendorf Art. No. 0030 120,094) are about 5 mg of the active ingredient weighed accurately and to a concentration of 5 g / l with PBS buffer pH 7.4 (e.g., 5 mg of active ingredient + 500 μl of PBS buffer pH 7.4).

Sample solution for solubility to 10 g / l in acetate buffer pH 4. 6: In a 2 ml Eppendorf Safe-Lock Tube (Eppendorf Art. No. 0030 120,094) are about 5 mg of the active ingredient weighed accurately and to a concentration of 5 g / l with acetate buffer pH 4.6 (for example 5 mg of active ingredient + 500 μl of acetate buffer pH 4.6).

Sample solution for solubility up to 10 g / l in water: In a 2 ml Eppendorf Safe-Lock Tube (Eppendorf Art. No. 0030 120,094), approximately 5 mg of the active ingredient are weighed exactly and added to water at a concentration of 5 g / l (e.g. mg active ingredient + 500 μl Water).

Execution:

The Sample solutions prepared in this way are heated for 24 hours at 1400 rpm by means of a temperature-controlled shaker (e.g. Eppendorf Thermomixer comfort Art. No. 5355 000.011 with exchange block Art. No. 5362.000.019) at 20 ° C shaken. From these solutions each 180 ul in Beckman Polyallomer Centrifuge Tubes (Art. No. 343621). These solutions are centrifuged for 1 hour at about 223,000 * g (e.g., Beckman Optima L-90K ultracentrifuge with Type 42.2 Ti rotor at 42,000 rpm). From every sample solution 100 μl of the supernatant decreased and 1: 5, 1: 100 and 1: 1000 with each used solvent (Water, PBS buffer 7.4 or acetate buffer pH 4.6) diluted. It is from any dilution a bottling in a suitable vessel for HPLC analysis performed.

analytics:

The Samples are analyzed by RP-HPLC. Is quantified over a Two-point calibration curve the test compound in DMSO. The solubility is expressed in mg / l.

Analysis sequence:

• 1. Calibrating solution 2.5 mg / ml
• 2. Calibration solution 20 μg / ml
• 3. Sample solution 1: 5
• 4. Sample solution 1: 100
• 5. Sample solution 1: 1000

HPLC method for acids:

• Agilent 1100 with DAD (G1315A), quat. Pump (G1311A), autosampler CTC HTS PAL, Degaser (G1322A) and Column Thermostat (G1316A); Column: Phenomenex Gemini C18, 50 × 2 mm, 5 μ; Temperature: 40 ° C; Eluent A: water / phosphoric acid pH 2; Eluent B: acetonitrile; Flow rate: 0.7 ml / min; Gradient: 0-0.5 min 85% A, 15% B; Ramp: 0.5-3 min 10% A, 90% B; 3-3.5 min 10% A, 90% B; Ramp: 3.5-4 min 85% A, 15% B; 4-5 min 85% A, 15% B.

HPLC method for bases:

• Agilent 1100 with DAD (G1315A), quat. Pump (G1311A), autosampler CTC HTS PAL, degasser (G1322A) and column thermostat (G1316A); Column: VDSoptilab Kromasil 100 C18, 60 × 2.1 mm, 3.5 μ; Temperature: 30 ° C; Elu ent A: water + 5 ml perchloric acid / l; Eluent B: acetonitrile; Flow rate: 0.75 ml / min; Gradient: 0-0.5 min 98% A, 2% B; Ramp: 0.5-4.5 min 10% A, 90% B; 4.5-6 min 10% A, 90% B; Ramp: 6.5-6.7 min 98% A, 2% B; 6.7-7.5 min 98% A, 2% B.

C. Exemplary embodiments for pharmaceutical compositions

The Compounds of the invention can as follows be converted into pharmaceutical preparations:

Tablet:

Composition:

100 mg of the compound according to the invention, 50 mg of lactose (monohydrate), 50 mg of corn starch (native), 10 mg of polyvinylpyrrolidone (PVP 25) (BASF, Ludwigshafen, Germany) and 2 mg of magnesium stearate.
Tablet weight 212 mg. Diameter 8 mm, radius of curvature 12 mm.

production:

The Mixture of compound according to the invention, Lactose and starch is with a 5% solution (m / m) of the PVP in water granulated. The granules will dry after drying mixed with the magnesium stearate for 5 minutes. This mixture will with a usual Pressed tablet press (format of the tablet see above). When Guideline for the compression is used a pressing force of 15 kN.

Orally administrable suspension:

Composition:

1000 mg of the compound of the invention, 1000 mg of ethanol (96%), 400 mg of Rhodigel ^® (xanthan gum of the firm FMC, Pennsylvania, USA) and 99 g of water.

one Single dose of 100 mg of the compound of the invention correspond 10 ml oral suspension.

production:

The Rhodigel is suspended in ethanol, the compound of the invention is added to the suspension. While stirring the addition of the water takes place. Until the completion of the swelling of the rhododendron is stirred for about 6 h.

Orally administrable solution:

Composition:

500 mg of the compound of the invention, 2.5 g polysorbate and 97 g polyethylene glycol 400. A single dose of 100 mg of the compound of the invention correspond to 20 g of oral solution.

production:

The inventive compound is suspended in the mixture of polyethylene glycol and polysorbate with stirring. The stirring process will be up to the full resolution the compound of the invention continued.

iv solution:

The inventive compound becomes in a concentration below the saturation solubility in a physiological acceptable solvent (e.g., isotonic saline, glucose solution 5% and / or PEG 400 solution 30%) solved. The solution is sterile filtered and placed in sterile and pyrogen-free injection containers bottled.

Claims (14)

Compound of the formula

in which A is a group of the formula

where R ^{1A is} hydrogen, fluorine, trifluoromethyl, hydroxy, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, C ₃ C ₆ -Cycloalkyloxy or C ₃ -C ₆ cycloalkylamino, wherein alkyl, alkoxy, alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyloxy, C ₃ -C ₆ -cycloalkylamino, (NC ₃ -C ₆ -cycloalkyl) (NC ₁ -C ₄ -alkyl) -amino and a 4- to 7- a saturated heterocyclic group which may contain a ring member of the series NR ²¹ , S or O, wherein R ^{21 is} hydrogen, C ₁ -C ₄ alkyl or C ₃ -C ₆ cycloalkyl, and the heterocycle may be substituted with one Substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ alkyl and oxo, R ^{1B is} hydrogen, hydroxy, amino, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy , C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, C ₃ -C ₆ -cycloalkyloxy or C ₃ -C ₆ -cycloalkylamino, wherein alkyl may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyloxy, C ₃ -C ₆ -cycloalkylamino, (NC ₃ -C ₆ -cycloalkyl) (NC ₁ -C ₄ -alkyl) -amino and a 4 - to 7-membered saturated heterocycle, which may contain a ring member from the series NR ²¹ , S or O, wherein R ^{21 is} hydrogen, C ₁ -C ₄ alkyl or C ₃ -C ₆ cycloalkyl, and the heterocycle substituted may be substituted with a substituent wherein the substituent is selected from the group consisting of hydroxy, amino, C ₁ -C ₄ alkyl and oxo, R ^{1C is} hydrogen, fluoro, cyano, hydroxy, amino, oxo, C ₁ -C ₄ Alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkylamino or C ₃ -C ₆ -cycloalkyl, R ^{1D represents} hydrogen, fluorine, cyano, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -Cycloalkyl, R ^{1E is} hydrogen, C ₁ -C ₄ alkyl or C ₃ -C ₆ cycloalkyl, and # is the point of attachment to the phenyl ring, m is the number 0, 1 or 2, and the (CH ₂ ) _m group in 1 or 2 position the phenyl ring is bonded, R ^{2 is} hydrogen, fluorine, chlorine, cyano, hydroxyl, amino, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, aminocarbonyl, C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl, R ^{3 is} hydrogen, fluorine, chlorine, cyano, hydroxyl, amino, Trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino, C ₃ -C ₆ -cycloalkyl, aminocarbonyl, C ₁ -C ₄ -alkoxycarbonyl or C ₁ -C ₄ -alkylaminocarbonyl, wherein alkyl, alkoxy and alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, C ₁ -C ₄ alkoxy, C ₃ -C _6- Cycloalkyloxy, pyrrolidinyl, pi peridinyl, morpholinyl, piperazinyl, 4-tetrahydropyranyl and -NR ¹⁴ R ¹⁵ ; wherein piperazinyl and piperidinyl on the nitrogen atom may be substituted with a substituent, wherein the substituent is selected from the group consisting of methyl and cyclopropyl, and R ^{14 is} hydrogen, C ₁ -C ₄ alkyl or C ₃ -C ₆ cycloalkyl, and R ^{15 is} hydrogen or C ₁ -C ₄ alkyl, R ⁴ and R ^{5 are} hydrogen, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ^{7 represent} hydrogen, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, R ^{8 represents} phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl or thienyl, wherein phenyl, pyridyl, pyrazinyl, pyrimidinyl and pyridazinyl are substituted by a substituent R ¹¹ and / or a substituent R ¹² or with two different substituents R ¹¹ or with two different substituents R ¹² , wherein R ¹¹ is bonded to a carbon atom which is not adjacent to a nitrogen atom in the ring, and for hydrogen, fluorine, chlorine , Cyano, ethynyl, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy or C ₃ -C ₆ cycloalkyl, R ¹² is bonded to a carbon atom adjacent to a nitrogen atom in the ring, and hydrogen, Amino, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkylamino or C ₃ -C ₆ cycloalkyl, and wherein thienyl is substituted with a substituent R ¹³ and a substituent R ¹⁶ , wherein R ^{13 is} attached to a carbon atom which is adjacent to the sulfur atom in the ring and is hydrogen, fluorine, chlorine, cyano, ethynyl, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy or C ₃ -C ₆ cycloalkyl, R ^{16 is} Is hydrogen, fluorine, chlorine, amino, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkylamino or C ₃ -C ₆ -cycloalkyl, R ^{9 is} hydrogen, F chloro, chloro, cyano, hydroxy, amino, trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy, C ₁ -C ₄ alkylamino, C ₃ -C ₆ cycloalkyl, aminocarbonyl, C ₁ C ₄ alkoxycarbonyl or C ₁ -C ₄ alkylaminocarbonyl, wherein alkyl, alkoxy and alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, C ₁ -C ₄ alkoxy, C ₃ -C ₆ -cycloalkyloxy, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, 4-tetrahydropyranyl and -NR ¹⁷ R ¹⁸ , wherein piperazinyl and piperidinyl may be substituted on the nitrogen atom with a substituent, wherein the substituent is selected from the group consisting of methyl and cyclopropyl and R ^{17 is} hydrogen, C ₁ -C ₄ -alkyl or C ₃ -C ₆ -cycloalkyl, and R ^{18 is} hydrogen or C ₁ -C ₄ -alkyl, R ^{10 is} hydrogen, fluorine, chlorine, cyano, Trifluoromethyl, trifluoromethoxy, C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy or C ₃ -C ₆ cycloalkyl, and w wherein R ^{9 is} attached to the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring, or wherein R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring, or one of its Salts, their solvates or the solvates of their salts. A compound according to claim 1, characterized in that A is a group of the formula

wherein R ^{1A is} hydrogen, fluorine, hydroxyl, amino, C ₁ -C ₄ alkyl, methoxy, ethoxy, tert-butoxy, methylamino, dimethylamino, ethylamino, diethylamino, tert-butylamino, cyclopropyl, cyclopropylmino or cyclopropyloxy in which alkyl, ethoxy, tert-butoxy, ethylamino, diethylamino and tert-butylamino may be substituted by a substituent, where the substituent is selected from the group consisting of hydroxyl, amino, methoxy, C ₁ -C ₄ -alkylamino, Cyclopropyloxy, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1-pyrrolidinyl, 1-piperidinyl, 4-piperidinyl, 4-morpholinyl, 1-piperazinyl and 4-tetrahydropyranyl, wherein 1-piperazinyl and 4-piperidinyl on the nitrogen atom may be substituted with a substituent wherein the substituent is selected from the group consisting of methyl and cyclopropyl, R ^{1B is} hydrogen, hydroxy, amino, C ₁ -C ₄ alkyl, methoxy, methylamino, dimethylamino or cyclopropyl wherein alkyl is substituted can be mi t is a substituent, wherein the substituent is selected from the group consisting of hydroxy, amino, methoxy, C ₁ -C ₄ alkylamino, cyclopropyloxy, cyclopropylamino, (N-cyclopropyl) (N-methyl) amino, 1-pyrrolidinyl, 1 Piperidinyl, 4-piperidinyl, 4-morpholinyl, 1-piperazinyl and 4-tetrahydropyranyl, wherein 1-piperazinyl and 4-piperidinyl may be substituted on the nitrogen atom with a substituent wherein the substituent is selected from the group consisting of methyl and cyclopropyl, R ^{1C is} hydrogen, fluoro, oxo or methyl, R ^{1D is} hydrogen, fluoro or methyl, and # is the point of attachment to the phenyl ring, m is the number 0, 1 or 2, and the (CH ₂ ) _m group is bonded to the phenyl ring in 1 or 2 position, R ^{2 is} hydrogen, fluorine, chlorine, cyano, hydroxy, C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy, R ^{3 is} hydrogen, fluorine, Chlorine, cyano, hydroxy, C ₁ -C ₄ -alkyl, C ₁ -C ₄ -alkoxy, C ₁ -C ₄ -alkoxymethyl, C ₁ -C ₄ -alkylamino, Cyc lopropyl, aminocarbonyl, C ₁ -C ₄ alkoxycarbonyl or C ₁ -C ₄ alkylaminocarbonyl, wherein alkyl, alkoxy and alkylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy, methoxy, 1- Pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, 1-piperazinyl and -NR ¹⁴ R ¹⁵ , where 1-piperazinyl may be substituted on the nitrogen atom by a substituent, the substituent being selected from the group consisting of methyl and cyclopropyl, and R ^{14 is} hydrogen, methyl or cyclopropyl, and R ^{15 is} hydrogen or methyl, R ⁴ and R ^{5 are} hydrogen, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ^{7 represent} hydrogen, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, R ^{8 represents} a group of the formula

where * is the point of attachment to the carbonyl group, R ^{11 is} fluorine, chlorine, ethynyl, methyl, ethyl, methoxy or ethoxy, R ^{12 is} amino, methyl, methylamino or dimethylamino, R ^{13 is} fluorine, chlorine, ethynyl, methyl, ethyl, methoxy or ethoxy, and R ¹⁶ is hydrogen, R ⁹ is hydrogen, fluorine, chlorine, cyano, methyl, methoxy, aminocarbonyl, methylaminocarbonyl or dimethylaminocarbonyl, with methyl and methoxy may be substituted with a substituent, whereby the substituent is selected from the group consisting of hydroxy, methoxy, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, 1-piperazinyl and -NR ¹⁷ R ¹⁸ , wherein 1-piperazinyl may be substituted on the nitrogen atom with a substituent, wherein the Substituent is selected from the group consisting of methyl and cyclopropyl, and R ^{17 is} hydrogen, methyl or cyclopropyl, and R ^{18 is} hydrogen or methyl, R ^{10 is} hydrogen, fluorine, chlorine, cyano, Trifluoromethyl, trifluoromethoxy, methyl or methoxy, and wherein R ^{9 is} attached to the 6-position and R ¹⁰ to the 7-position of the isoindoline ring, or where R ^{9 is} at the 7-position and R ^{10 is} at the 6-position Isoindolin ring bound. Compound according to one of claims 1 or 2, characterized in that A represents a group of formula

wherein R ^{1A is} hydrogen, fluorine, hydroxyl, amino, methyl, ethyl, iso-propyl, methoxy, ethoxy, methylamino, dimethylamino, ethylamino, diethylamino or cyclopropylamino, wherein methyl, ethyl, iso-propyl, ethoxy, ethylamino and Dethylamino may be substituted with a substituent, wherein the substituent is selected from the group consisting of hydroxy; Amino, methoxy, methylamino, dimethylamino, cyclopropylamino, (N-cyclopropyl) (N -methyl) amino, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl and 1-piperazinyl, wherein 1-piperazinyl on the nitrogen atom may be substituted with a substituent wherein the substituent is selected from the group consisting of methyl and cyclopropyl, R ^{1B is} hydrogen, hydroxy, amino, methyl, ethyl, iso-propyl or cyclopropyl, wherein ethyl and iso-propyl may be substituted with a substituent, wherein the Substituent is selected from the group consisting of hydroxy, amino, methoxy, methylamino, dimethylamino, cyclopropylamino, (N-cyclopropyl) (N-methyl) amino, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl and 1-piperazinyl, wherein 1 -Piperazinyl may be substituted on the nitrogen atom with a substituent, wherein the substituent is selected from the group consisting of methyl and cyclopropyl, R ^{1C is} hydrogen, fluorine, oxo or methyl, R ^{1D is} hydrogen, fluorine od it is methyl, and # is the point of attachment to the phenyl ring, m is the number 1, and the (CH ₂ ) _m group is attached in 1 or 2 position to the phenyl ring, R ^{2 is} hydrogen, R ³ is hydrogen, fluorine, chlorine, cyano, methyl, ethyl, n-propyl, methoxy, ethoxy or methoxymethyl, R ⁴ and R ^{5 are} hydrogen, and R ⁶ and R ⁷ together with the carbon atom to which they are attached, form a carbonyl group, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ^{7 represent} hydrogen, or R ⁴ and R ⁵ together with the carbon atom to which they are attached are, form a carbonyl group, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group; R ^{8 represents} a group of the formula

where * is the point of attachment to the carbonyl group, R ^{13 is} fluoro, chloro or methyl, and R ^{16 is} hydrogen, R ^{9 is} hydrogen, R ^{10 is} hydrogen, and wherein R ^{9 is} at the 6-position and R ^{10 is} attached to the 7-position of the isoindoline ring, or where R ^{9 is} attached to the 7-position and R ^{10 is} attached to the 6-position of the isoindoline ring. Compound according to one of claims 1 to 3, characterized in that A represents a group of formula

where # is the point of attachment to the phenyl ring, m is the number 1, and the (CH ₂ ) _m group is attached in 1 or 2 position to the phenyl ring, R ^{2 is} hydrogen, R ^{3 is} hydrogen , Fluorine, chlorine, cyano or methyl, R ⁴ and R ^{5 are} hydrogen, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ^{7 are} hydrogen, or R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ⁷ together with the carbon atom to which they are attached form a carbonyl group, R ^{8 represents} a group of the formula

where * is the point of attachment to the carbonyl group, R ^{13 is} chlorine, and R ^{16 is} hydrogen, R ^{9 is} hydrogen, R ^{10 is} hydrogen, and wherein R ⁹ to the 6-position and R ¹⁰ to the 7-position of the isoindoline ring is bound, or wherein R ^{9 is} attached to the 7-position and R ¹⁰ to the 6-position of the isoindoline ring. Process for the preparation of a compound of the formula (I) or one of its salts, of its solvates or of the solvates of its salts according to Claim 1, characterized in that [A] is a compound of the formula

in which m, R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} the meaning given in claim 1, with a compound of formula AH (III), in which A has the meaning given in claim 1, or [B] a compound of the formula

in which R ⁸ , A ⁹ and R ^{10 have} the meaning given in claim 1, with a compound of the formula

in which A, m, R ² and R ^{3 have} the meaning given in claim 1, to give a compound of formula (I) in which R ⁴ and R ⁵ together with the carbon atom to which they are attached form a carbonyl group, and R ⁶ and R ⁷ are reacted together with the carbon atom to which they are attached to form a carbonyl group. A compound according to any one of claims 1 to 4 for the treatment and / or prophylaxis of diseases. Use of a compound according to any one of claims 1 to 4 for the manufacture of a medicament for the treatment and / or prophylaxis of diseases. Use of a compound according to any one of claims 1 to 4 for the manufacture of a medicament for the treatment and / or prophylaxis of thromboembolic disorders. Use of a compound according to any one of claims 1 to 4 for the prevention of blood coagulation in vitro. Medicament containing a compound after one the claims 1 to 4 in combination with an inert, non-toxic, pharmaceutical suitable excipient. Medicament containing a compound after one the claims 1 to 4 in combination with another active ingredient. Medicament according to claim 10 or 11 for the treatment and / or prophylaxis of thromboembolic Diseases. Method for the treatment and / or prophylaxis of using thromboembolic diseases in humans and animals an anticoagulatory effective amount of at least one compound one of the claims 1 to 4, a medicament according to any one of claims 10 to 12 or a medicament obtained according to claim 7 or 8. Method for preventing blood coagulation in in vitro, characterized in that an anticoagulatory effective Amount of a compound according to any one of claims 1 to 4 is added.