Triaza-spiropiperidine derivatives
    62.
    发明授权
    Triaza-spiropiperidine derivatives 失效
    三氮杂 - 哌啶衍生物

    公开(公告)号:US07189850B2

    公开(公告)日:2007-03-13

    申请号:US10967534

    申请日:2004-10-18

    IPC分类号: C07D471/10

    CPC分类号: C07D471/10

    摘要: The invention relates to compounds of the general formula wherein A-A is —CH2—CH2—, —CH2—CH2—CH2—, —CH2—O— or —O—CH2—; and X, R1, R2, R3, R4, R5, R6, n, and p are as defined herein, or a pharmaceutically acceptable salt thereof for the treatment of psychoses, pain, neurodegenerative dysfunction in memory and learning, schizophrenia, dementia and other diseases in which cognitive processes are impaired, such as attention deficit disorders or Alzheimer's disease.

    摘要翻译: 本发明涉及以下通式的化合物:其中AA是-CH 2 -CH 2 - , - CH 2 -CH 2 -CH 2 - , - CH 2 -O-O-或-O-CH 2 - ; - 和X,R 1,R 2,R 3,R 4,R 5, 本发明中,n和p如本文所定义,或其药学上可接受的盐用于治疗精神病,疼痛,记忆和学习中的神经变性功能障碍,精神分裂症,痴呆等疾病 哪些认知过程受损,如注意力缺陷障碍或阿尔茨海默病。

    Benzoyl-tetrahydropiperidine derivatives
    65.
    发明申请
    Benzoyl-tetrahydropiperidine derivatives 失效
    苯甲酰基 - 四氢哌啶衍生物

    公开(公告)号:US20060148797A1

    公开(公告)日:2006-07-06

    申请号:US11302403

    申请日:2005-12-13

    IPC分类号: A61K31/5377 C07D413/02

    CPC分类号: C07D211/70

    摘要: The present invention relates to compounds of formula I wherein R1, R2, and Ar; are as defined in the specification. The invention also provides pharmaceutically acceptable acid addition salts thereof and methods for the treatment of neurological and neuropsychiatric disorders, such as schizophrenia, cognitive impairment, and Alzheimer's disease.

    摘要翻译: 本发明涉及式I化合物,其中R 1,R 2,R 2和Ar; 如说明书中所定义。 本发明还提供其药学上可接受的酸加成盐以及用于治疗神经和神经精神疾病如精神分裂症,认知障碍和阿尔茨海默病的方法。

    Diaza-spiropiperidine derivatives
    67.
    发明申请
    Diaza-spiropiperidine derivatives 失效
    二氮杂 - 哌啶衍生物

    公开(公告)号:US20050154001A1

    公开(公告)日:2005-07-14

    申请号:US11028281

    申请日:2005-01-03

    IPC分类号: C07D471/10 A61K31/4747

    CPC分类号: C07D471/10

    摘要: The present invention relates to compounds of formula wherein A-B is —CH2—CH2—, —CH2—O— or —O—CH2—; X is hydrogen or hydroxy; R1 is aryl, optionally substituted by one or two substituents selected from the group consisting of halogen, lower alkyl, cyano, CF3, —OCF3, lower alkoxy, —SO2-lower alkyl and heteroaryl; R2 is aryl, optionally substituted by one or two substituents selected from the group consisting of halogen, lower alkyl, CF3, and lower alkoxy; R3 is hydrogen or lower alkyl; n is 0, 1 or 2; or a pharmaceutically active salt thereof. The compounds of the invention may be used in the treatment of neurological and neuropsychiatric disorders.

    摘要翻译: 本发明涉及下式的化合物其中AB是-CH 2 -CH 2 - , - CH 2 -O - 或-O- CH 2 - ; X是氢或羟基; R 1是芳基,任选被一个或两个选自卤素,低级烷基,氰基,CF 3,-OCF 3, 低级烷氧基,-SO 2 - 低级烷基和杂芳基; R 2是任选被一个或两个选自卤素,低级烷基,CF 3 N 3和低级烷氧基的取代基取代的芳基; R 3是氢或低级烷基; n为0,1或2; 或其药物活性盐。 本发明的化合物可用于治疗神经和神经精神障碍。