3-Heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide Derivatives, Their Preparation and Therapeutic Use
    3.
    发明申请
    3-Heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide Derivatives, Their Preparation and Therapeutic Use 有权
    3-杂芳基-3,5-二氢-4-氧代-4H-哒嗪并[4,5-B]吲哚-1-甲酰胺衍生物及其制备和治疗用途

    公开(公告)号:US20080249098A1

    公开(公告)日:2008-10-09

    申请号:US12140608

    申请日:2008-06-17

    IPC分类号: A61K31/5025 A61P25/00

    CPC分类号: C07D487/04 C07D209/42

    摘要: A subject-matter of the invention is the compounds of general formula (I) in which X represents a hydrogen or halogen atom; R1 represents a hydrogen atom or a (C1-C4)alkyl group; R2 and R3 each represent, independently of one another, a hydrogen atom or a (C1-C4)alkyl group or else R2 and R3 form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and Het represents a heteroaromatic group of pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl or pyridazinyl type, it being possible for the heteroaromatic group to carry one or more halogen atoms and/or one or more (C1-C4) alkyl or (C1-C4) alkoxy groups; in the form of bases, of addition salts with acids, of solvates or of hydrates, the pharmaceutical compositions comprising them, processes for their preparation and synthetic intermediates.

    摘要翻译: 本发明的主题是通式(I)的化合物,其中X表示氢或卤素原子; R 1表示氢原子或(C 1 -C 4 -C 4)烷基; R 2和R 3各自独立地表示氢原子或(C 1 -C 4)烷基, 或者R 2和R 3形式,与携带它们的氮原子一起形成吡咯烷基,哌啶基,吗啉基或4-烷基哌嗪基; 并且Het表示吡啶基,1-氧化吡啶基,喹啉基,异喹啉基,嘧啶基,吡嗪基或哒嗪基的杂芳族基团,杂芳基可以携带一个或多个卤素原子和/或一个或多个(C 1 C 1 -C 4烷基或(C 1 -C 4 -C 4)烷氧基; 以碱的形式,与酸,溶剂合物或水合物的加成盐,包含它们的药物组合物,其制备方法和合成中间体。

    3-heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide derivatives, their preparation and therapeutic use
    4.
    发明授权
    3-heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide derivatives, their preparation and therapeutic use 有权
    3-杂芳基-3,5-二氢-4-氧代-4H-哒嗪并[4,5-B]吲哚-1-甲酰胺衍生物,其制备和治疗用途

    公开(公告)号:US07402682B2

    公开(公告)日:2008-07-22

    申请号:US11427508

    申请日:2006-06-29

    CPC分类号: C07D487/04 C07D209/42

    摘要: A subject-matter of the invention is the compounds of general formula (I) in which X represents a hydrogen or halogen atom; R1 represents a hydrogen atom or a (C1-C4)alkyl group; R2 and R3 each represent, independently of one another, a hydrogen atom or a (C1-C4)alkyl group or else R2 and R3 form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and Het represents a heteroaromatic group of pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl or pyridazinyl type, it being possible for the heteroaromatic group to carry one or more halogen atoms and/or one or more (C1-C4)alkyl or (C1-C4)alkoxy groups; in the form of bases, of addition salts with acids, of solvates or of hydrates, the pharmaceutical compositions comprising them, processes for their preparation and synthetic intermediates.

    摘要翻译: 本发明的主题是通式(I)的化合物,其中X表示氢或卤素原子; R 1表示氢原子或(C 1 -C 4 -C 4)烷基; R 2和R 3各自独立地表示氢原子或(C 1 -C 4)烷基, 或者R 2和R 3形式,与携带它们的氮原子一起形成吡咯烷基,哌啶基,吗啉基或4-烷基哌嗪基; 并且Het表示吡啶基,1-氧化吡啶基,喹啉基,异喹啉基,嘧啶基,吡嗪基或哒嗪基的杂芳族基团,杂芳基可以携带一个或多个卤素原子和/或一个或多个(C 1 C 1 -C 4烷基或(C 1 -C 4 -C 4)烷氧基; 以碱的形式,与酸,溶剂合物或水合物的加成盐,包含它们的药物组合物,其制备方法和合成中间体。

    3-Heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide derivatives, their preparation and therapeutic use
    8.
    发明授权
    3-Heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-B]indole-1-carboxamide derivatives, their preparation and therapeutic use 有权
    3-杂芳基-3,5-二氢-4-氧代-4H-哒嗪并[4,5-b]吲哚-1-甲酰胺衍生物,其制备和治疗用途

    公开(公告)号:US07569567B2

    公开(公告)日:2009-08-04

    申请号:US12140608

    申请日:2008-06-17

    IPC分类号: A61K31/503 C07D487/02

    CPC分类号: C07D487/04 C07D209/42

    摘要: A subject-matter of the invention is the compounds of general formula (I) in which X represents a hydrogen or halogen atom; R1 represents a hydrogen atom or a (C1-C4)alkyl group; R2 and R3 each represent, independently of one another, a hydrogen atom or a (C1-C4)alkyl group or else R2 and R3 form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and Het represents a heteroaromatic group of pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl or pyridazinyl type, it being possible for the heteroaromatic group to carry one or more halogen atoms and/or one or more (C1-C4) alkyl or (C1-C4) alkoxy groups; in the form of bases, of addition salts with acids, of solvates or of hydrates, the pharmaceutical compositions comprising them, processes for their preparation and synthetic intermediates.

    摘要翻译: 本发明的主题是通式(I)的化合物,其中X表示氢或卤素原子; R1表示氢原子或(C1-C4)烷基; R2和R3各自独立地表示氢原子或(C1-C4)烷基,或者R2和R3与携带它们的氮原子一起形成吡咯烷基,哌啶基,吗啉基或4-烷基哌嗪基; 并且Het表示吡啶基,1-氧化吡啶基,喹啉基,异喹啉基,嘧啶基,吡嗪基或哒嗪基的杂芳族基团,杂芳基可以携带一个或多个卤素原子和/或一个或多个(C 1 -C 4)烷基 或(C 1 -C 4)烷氧基; 以碱的形式,与酸,溶剂合物或水合物的加成盐,包含它们的药物组合物,其制备方法和合成中间体。

    3-heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-b] indole-1-acetamide derivatives, preparation and use thereof in medicaments
    10.
    发明授权
    3-heteroaryl-3,5-dihydro-4-oxo-4H-pyridazino[4,5-b] indole-1-acetamide derivatives, preparation and use thereof in medicaments 有权
    3-杂芳基-3,5-二氢-4-氧代-4H-哒嗪并[4,5-b]吲哚-1-乙酰胺衍生物,其药物的制备和用途

    公开(公告)号:US07235554B2

    公开(公告)日:2007-06-26

    申请号:US10509695

    申请日:2003-04-02

    IPC分类号: C07D487/04 A61K31/5025

    CPC分类号: C07D209/42 C07D487/04

    摘要: The invention provides compounds of general formula (I) in which X represents a hydrogen or halogen atom; R1 represents a hydrogen atom or a (C1-C4)alkyl group; R2 and R3 each independently of one another represent a hydrogen atom or a (C1-C4)alkyl group, or else R2 and R3, together with the nitrogen atom bearing them, form a pyrrolidinyl, piperidinyl, morpholinyl or 4-(C1-C4)alkylpiperazinyl group; and Het represents a heteroaromatic group of pyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl or pyridazinyl type which may carry one or more halogen atoms and/or one or more (C1-C4)alkyl and/or (C1-C4)alkoxy groups; in the form of bases, addition salts with acids, solvates or hydrates; the pharmaceutical compositions comprising them, processes for preparing them, and synthesis intermediates.

    摘要翻译: 本发明提供通式(I)的化合物,其中X表示氢或卤素原子; R 1表示氢原子或(C 1 -C 4 -C 4)烷基; R 2和R 3各自独立地表示氢原子或(C 1 -C 4)烷基, )烷基,或者R 2和R 3 3与带有它们的氮原子一起形成吡咯烷基,哌啶基,吗啉基或4-(C 1 C 4 -C 4烷基哌嗪基; 并且Het表示可携带一个或多个卤素原子和/或一个或多个(C 1 -C 4)烷基的吡啶基,喹啉基,异喹啉基,嘧啶基,吡嗪基或哒嗪基的杂芳族基团, (C 1 -C 4)烷基和/或(C 1 -C 4 -C 4)烷氧基; 碱的形式,与酸,溶剂合物或水合物的加成盐; 包含它们的药物组合物,其制备方法和合成中间体。