Quinolinone-Carboxamide Compounds as 5-Ht4 Receptor Agonists
    3.
    发明申请
    Quinolinone-Carboxamide Compounds as 5-Ht4 Receptor Agonists 有权
    喹啉酮 - 甲酰胺化合物作为5-Ht4受体激动剂

    公开(公告)号:US20070281970A1

    公开(公告)日:2007-12-06

    申请号:US11547790

    申请日:2005-04-06

    摘要: The invention provides novel quinolinone-carboxamide 5-HT4 receptor agonist compounds of Formula (I). The invention also provides pharmaceutical compositions comprising such compounds, the use such compounds to treat diseases associated with 5-HT4 receptor activity, and processes and intermediates useful for preparing such compounds. Wherein; R1 is hydrogen, halo, hadroxy, C1-4 alkyl, or C1-4 alkoxy; R2 is C3-4 alkyl, or C3-6cycloakyl; R3 is hydrogen or C1-3 alkyl: R4 is —S(O)2 R6 or —C(O)R7; R5 is hydrogen, C1-3alkyl, C2-3 alkyl subtituted with —OH or C1-3 alkoxy, or —CH2-pyrydyl; R6 is C1-3 alkyl; or R5 and R6 taken together from C3-4 alkylenyl; and R7 is hydrogen, C1-3alkyl, or pyrydyl; or pharmaceutically-acceptable salt or solvate or stereoisomer thereof.

    摘要翻译: 本发明提供式(I)的新型喹啉酮 - 甲酰胺5-HT 4受体激动剂化合物。 本发明还提供包含这些化合物的药物组合物,使用这些化合物治疗与5-HT 4受体活性相关的疾病,以及可用于制备这些化合物的方法和中间体。 其中; R 1是氢,卤素,羟基,C 1-4 - 烷基或C 1-4 - 烷氧基; R 2是C 3-4 - 烷基或C 3-6环烷基; R 3是氢或C 1-3烷基:R 4是-S(O)2 R 2, 或-C(O)R 7; R 5是氢,C 1-3烷基,被-OH或C 1-3烷基取代的C 2-3-3烷基, 烷基,或-CH 2 - 吡啶基; R 6是C 1-3烷基; 或R 5和R 6一起从C 3-4 - 亚烷基取代; R 7是氢,C 1-3烷基或吡喃基; 或其药学上可接受的盐或溶剂合物或立体异构体。