发明申请
WO2011143155A1 SUBSTITUTED N-HETEROARYL TETRAHYDRO-ISOQUINOLINE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF
审中-公开
基本信息:
- 专利标题: SUBSTITUTED N-HETEROARYL TETRAHYDRO-ISOQUINOLINE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF
- 专利标题(中):取代的N-异佛尔酮四氢异喹啉衍生物,其制备和治疗用途
- 申请号:PCT/US2011/035835 申请日:2011-05-10
- 公开(公告)号:WO2011143155A1 公开(公告)日:2011-11-17
- 发明人: GAO, Zhongli , HARTUNG, Ryan
- 申请人: SANOFI , GAO, Zhongli , HARTUNG, Ryan
- 申请人地址: 174 avenue de France F-75013 Paris FR
- 专利权人: SANOFI,GAO, Zhongli,HARTUNG, Ryan
- 当前专利权人: SANOFI,GAO, Zhongli,HARTUNG, Ryan
- 当前专利权人地址: 174 avenue de France F-75013 Paris FR
- 代理机构: LIN, Jiang et al.
- 优先权: FR1061064 20101222; US61/333,385 20100511
- 主分类号: C07D401/14
- IPC分类号: C07D401/14 ; C07D403/14 ; C07D413/14 ; A61K31/4709 ; A61P25/00
摘要:
The present invention discloses and claims a series of substituted N-heteroaryl tetrahydro-isoquinoline derivatives of Formula (I). Wherein R, R 1 , R 2 , X, m, n and p are as described herein. More specifically, the compounds of this invention are modulators of H3 receptors and are, therefore, useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases modulated by H3 receptors including diseases associated with the central nervous system. Additionally, this invention also discloses methods of preparation of substituted N-heteroaryl tetrahydro-isoquinoline derivatives of Formula (I) and intermediates therefor.
摘要(中):
本发明公开并要求一系列式(I)的取代的N-杂芳基四氢 - 异喹啉衍生物。 其中R,R1,R2,X,m,n和p如本文所述。 更具体地,本发明的化合物是H3受体的调节剂,因此可用作药剂,特别是用于治疗和/或预防由H3受体调节的各种疾病,包括与中枢神经系统相关的疾病。 此外,本发明还公开了制备式(I)的取代的N-杂芳基四氢 - 异喹啉衍生物及其中间体的方法。
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D401/00 | 杂环化合物,含有两个或更多个杂环,以氮原子作为仅有的杂环原子,至少有1个环是仅含有1个氮原子的六元环 |
--------C07D401/14 | .含有3个或更多个杂环 |