Azole derivatives
    1.
    发明授权
    Azole derivatives 失效
    唑衍生物

    公开(公告)号:US5290776A

    公开(公告)日:1994-03-01

    申请号:US886798

    申请日:1992-05-21

    CPC分类号: C07D487/04

    摘要: A compound of the formula I ##STR1## wherein: R.sup.1 is hydrogen, (1-6C)alkyl, or (1-4C)alkanoyl;R.sup.2 is phenyl, a C-linked aromatic 5- or 6-membered heterocyclic ring containing one of oxygen and sulphur and/or one or two nitrogen, or (1-8C)alkyl, alkenyl or alkynyl unsubstituted or substituted by a phenyl or a C-linked aromatic 5- or 6-membered heterocylic ring containing one of oxygen and sulphur and/or one or two nitrogen, any phenyl being unsubstituted or substituted by one, two or three of (1-4C)alkyl, (1-4C)alkoxy, halogen, trifluoromethyl, hydroxy, benzyloxy and (1-5C)alkanoyloxy;A is N or CT in which T is hydrogen or (1-4C)alkyl;or a pharmaceutically acceptable salt thereof, processes for the manufacture of the compounds, and pharmaceutical compositions containing them. The compounds are useful as adenosine antagonists.

    摘要翻译: 式I化合物(*化学结构*)Ⅰ其中:R1为氢,(1-6C)烷基或(1-4C)烷酰基; R2是苯基,含有氧和硫之一和/或一个或两个氮的C-连接的芳香族5-或6-元杂环,或未被取代或被苯基取代或(1-8C)烷基, 含有一个氧和硫和/或一个或两个氮的C连接的芳族5-或6-元杂环,任何未被取代或被一个,两个或三个(1-4C)烷基取代的苯基(1-4C )烷氧基,卤素,三氟甲基,羟基,苄氧基和(1-5C)烷酰氧基; A是N或CT,其中T是氢或(1-4C)烷基; 或其药学上可接受的盐,用于制备化合物的方法和含有它们的药物组合物。 这些化合物可用作腺苷拮抗剂。