首页> 外国专利> Compound N - (((1S, 4S, 6S) - 3 - (2 - piridinilcarbonil) 3-azabicyclo hept-3-ene (4,1.0) - 4-yl) methyl) - 2 - heteroarilamina, their use for the preparation of a Medicament for the treatment of a disease that requires a Human Orexin receptor antagonist Pharmaceutical composition containing same and

Compound N - (((1S, 4S, 6S) - 3 - (2 - piridinilcarbonil) 3-azabicyclo hept-3-ene (4,1.0) - 4-yl) methyl) - 2 - heteroarilamina, their use for the preparation of a Medicament for the treatment of a disease that requires a Human Orexin receptor antagonist Pharmaceutical composition containing same and

机译:化合物N-(((1S,4S,6S)-3-(2-吡啶并二甲腈)3-氮杂双环庚-3-烯(4,1.0)-4-基)甲基)-2-杂芳基,其用于制备用于治疗需要人类Orexin受体拮抗剂的疾病的药物

摘要

(1) was prepared from n - [(1s, 4S, 6S) - 3 - (2-piridinilcobonil) - 3-azabicil [4.1.0] hept-4-ii] met} - 2-heteromorphic amine,wherein: Het is a heteroaryl group selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl or pyrazinyl, said heteroaryl group being optionally substituted with 1, 2 or 3 substituents independently selected from the group consisting of: C1-4 alkyl, halogen , C1-4 alkoxy, C1-4 halogenoalkyl, C1-4 halogenoalkoxy and cyano; R1 is C1-4 alkyl, halogen, C1-4 alkoxy, C1-4 halogenoalkyl, C1-4 halogenoalkoxy, cyano, C1-4-SO2 alkyl, C3-8-SO2 cycloalkyl, C3-8-CH2SO2 cycloalkyl, phenyl or a group 5 or 6-membered heterocyclyl containing 1, 2 or 3 atoms selected from N, O or S,whose phenyl or heterocyclyl group is optionally substituted with C1-4 alkyl, halogen, C1-4 alkoxy, C1-4 halogenoalkyl, C1-4 halogenoalkoxy, or cyano, R2 is C1-4 alkyl, halogen, C1-4 alkoxy, C1 halogenalkyl -4, C1-4 halogenoalkoxy, cyano, phenyl or a 5- or 6-membered heterocyclyl group containing 1, 2 or 3 atoms selected from N, O or S, whose phenyl or heterocyclyl group is optionally substituted with C1-4 alkyl, halogen, C1-4 alkoxy, C1-4 halogenoalkyl, C1-4 halogenoalkoxy, or cyano, R3 is C1-4 alkyl, halogen, C1-4 alkoxy, C1-4 halogenoalkyl, C1-4 halogenoalkoxy, or cyano, m is 0 or 1; and n is 0 or 1;Or a pharmaceutically acceptable salt 2. Use this compound to prepare useful drugs for the treatment of diseases or disorders. This drug requires the antagonists of the human oregiline receptor and the pharmaceutical ingredients including this drug.
机译:(1)是从n-[(1s,4S,6S)-3-(2-哌啶子乙酮)-3-氮杂双环[4.1.0] hept-4-ii]制备的}-2-杂亚胺制备的,其中:Het杂芳基是选自吡啶基,嘧啶基,哒嗪基或吡嗪基的杂芳基,所述杂芳基任选地被1、2或3个独立地选自C 1-4烷基,卤素,C 1-4烷氧基的取代基取代。 ,C 1-4卤代烷基,C 1-4卤代烷氧基和氰基; R1是C1-4烷基,卤素,C1-4烷氧基,C1-4卤代烷基,C1-4卤代烷氧基,氰基,C1-4-SO2烷基,C3-8-SO2环烷基,C3-8-CH2SO2环烷基,苯基或含有1、2或3个选自N,O或S的原子的5或6元杂环基,其苯基或杂环基任选被C1-4烷基,卤素,C1-4烷氧基,C1-4卤代烷基,C1- 4个卤代烷氧基或氰基,R 2为C 1-4烷基,卤素,C 1-4烷氧基,C 1卤代烷基-4,C 1-4卤代烷氧基,氰基,苯基或含有1、2或3个原子的5或6元杂环基选自N,O或S,其苯基或杂环基任选地被C 1-4烷基,卤素,C 1-4烷氧基,C 1-4卤代烷基,C 1-4卤代烷氧基或氰基取代,R 3是C 1-4烷基,卤素C 1-4烷氧基,C 1-4卤代烷基,C 1-4卤代烷氧基或氰基,m为0或1; n为0或1;或为药学上可接受的盐2。使用该化合物制备用于治疗疾病或失调的有用药物。该药物需要人类Oregiline受体的拮抗剂以及包括该药物在内的药物成分。

著录项

  • 公开/公告号AR074426A1

    专利类型

  • 公开/公告日2011-01-19

    原文格式PDF

  • 申请/专利权人 GLAXO GROUP LIMITED;

    申请/专利号AR2009P104605

  • 发明设计人

    申请日2009-11-30

  • 分类号C07D401/12;C07D401/14;C07D413/12;C07D413/14;C07D417/14;A61K31/4427;A61K31/55;A61P3/04;A61P25/00;

  • 国家 AR

  • 入库时间 2022-08-21 18:07:27

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