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    • 22. 发明授权
    • Thienopyridine derivatives, their production and use
    • 噻吩并吡啶衍生物,其生产和使用
    • US07067527B2
    • 2006-06-27
    • US10662165
    • 2003-09-03
    • Tsuneo YasumaAtsuo BabaHaruhiko MakinoIsao AokiToshiaki Nagata
    • Tsuneo YasumaAtsuo BabaHaruhiko MakinoIsao AokiToshiaki Nagata
    • C07D495/14A61K31/38
    • C07D495/04C07D495/14
    • The present invention provides thienopyridine derivatives, which are useful as anti-inflammatory drugs, particularly as remedies for arthritis; processes for producing them, and pharmaceutical compositions containing them. The thienopyridine derivatives are represented by the formula (I): wherein G is a halogen atom, hydroxyl group, an optionally substituted amino group, etc.; alk is an optionally substituted lower alkylene group; X is O, S, —(CH2)q—, etc.; R is an optionally substituted amino group, etc.; ring B is an optionally substituted Y-containing 5- to 8-membered ring whose ring constituent atoms contain no nitrogen atom; Y is O, S, a group of (wherein Ra, Rb and Rc are the same or different and, each is H, a halogen atom, an optionally substituted hydrocarbon group, etc.), etc.; and ring A may be substituted.
    • 本发明提供可用作抗炎药物的噻吩并吡啶衍生物,特别是作为关节炎的补救剂; 制备它们的方法和含有它们的药物组合物。 噻吩并吡啶衍生物由式(I)表示:其中G是卤素原子,羟基,任选取代的氨基等; 烷基是任选取代的低级亚烷基; X是O,S, - (CH 2 CH 2)q - 等; R是任选取代的氨基等; 环B是任选取代的含有Y的5至8元环,其环组成原子不含氮原子; Y是O,S,(其中Ra,Rb和Rc相同或不同,并且各自为H,卤素原子,任选取代的烃基等)等; 并且环A可以被取代。