首页> 外国专利> Compound, Pharmaceutical Composition and use of the compound in the manufacture of a Medicament for the treatment of Cognitive disorder related to or affected by the Histamine Receptor 3 (H3) and Process for the preparation of the compound

Compound, Pharmaceutical Composition and use of the compound in the manufacture of a Medicament for the treatment of Cognitive disorder related to or affected by the Histamine Receptor 3 (H3) and Process for the preparation of the compound

机译:该化合物,药物组合物以及该化合物在制备用于治疗与组胺受体3(H3)相关或受其影响的认知障碍的药物中的用途以及该化合物的制备方法

摘要

A compound used to treat central nervous system disorders associated with or affected by histamine-3 receptors. 1. Formula 1 compounds characterized by X1 as (cr4r5) P, Co or O; x2a and x2bson, each h or formed at the same time = O; m as 0; 1 or 2; n as 2; 3 or 4; P as 0; 1 or 2; Q as 1; 2 or 3; R1 and R2 as independent h, halogen or a group of tar or halide, each group of alternative; R3 is nr6r7, or a set of asphalt, cyclo armour, cyclo armour, cyclo armour, cyclo armour, cyclo armour or heterogeneous, each set of alternative conditionsWhen x2a and x2bse combine to form = O and P = 0, R3 is not quinoxalinil-2 (1H) - ona, or 1.3.4-oxadiazol; when x2a and x2b are h and P, R3 is not 1.2.4-triazol-5 (4h) - ona; R4 and R5 are independent h or a group of alternative bitumen or cyclopentadiene; R6 and R7 are independent h or a group of bitumen, alquenilo, alcoxi, cyclopentadiene, cyclopentadiene, cyclopentadienylEach optional substitution group or R6 and R7 of arilo or heteromorphism can form a 4-a7-selective substitution ring with the atoms attached to them, which can selectively contain one or two additional heteroatoms selected from n, The aromatic ring system of o o o o s or 9-A 15 can optionally be composed of two or three mixed or three substituted two or three ring aromatic ring members composed of extra heteroatoms selected from n or s, or a stereoheteroatom, Taurus or salt acceptable for drugs.
机译:一种化合物,用于治疗与组胺3受体相关或受其影响的中枢神经系统疾病。 1.式1化合物,其特征在于X 1为(cr4r5)P,Co或O; x2a和x2bson,每个h或同时形成= O; m为0; 1或2; n为2; 3或4; P为0; 1或2; Q为1; 2或3; R1和R2为独立的h,卤素或一组焦油或卤化物,每组可替代; R3为nr6r7,或一组沥青,环甲,环甲,环甲,环甲,环甲或非均质,每组替代条件当x2a和x2bse结合形成= O和P = 0时,R3不是喹喔啉2(1H)-ona,或1.3.4-恶二唑;当x2a和x2b是h和P时,R3不是1.2.4-triazol-5(4h)-ona; R4和R5是独立的h或一组替代的沥青或环戊二烯; R 6和R 7是独立的h或一组沥青,alquenilo,alcoxi,环戊二烯,环戊二烯,环戊二烯基每个任选取代基或arilo或异构的R6和R7可以形成一个与原子相连的4-a7选择性取代环,其中可以选择性地包含一个或两个选自n的额外杂原子。oooos或9-A 15的芳族环系统可以任选地由两个或三个混合的或三个取代的两个或三个环芳族环成员组成,该芳族环成员选自n或n或药物可接受的立体杂原子,金牛座或盐。

著录项

  • 公开/公告号AR068423A1

    专利类型

  • 公开/公告日2009-11-18

    原文格式PDF

  • 申请/专利权人 WYETH;

    申请/专利号AR2008P103964

  • 申请日2008-09-12

  • 分类号C07D401/04;C07D401/06;C07D401/14;C07D403/04;C07D403/06;C07D405/06;C07D405/12;C07D405/14;C07D217/12;A61K31/472;A61K31/4725;A61P25/00;

  • 国家 AR

  • 入库时间 2022-08-21 18:47:36

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