Triazolyl- and imidazolyl-substituted fluoroalkane derivatives, process for their preparation and pharmaceutical compositions containing them
申请人:SCHERING CORPORATION
公开号:EP0122452A1
公开(公告)日:1984-10-24
The invention relates to novel compounds of the general formula
wherein n is zero or 1,
A is X-substituted phenyl or X-substituted thienyl (the phenyl and thienyl group containing 1 2 or 3 substituents X) or, provided n is 1 A can also be OR', SR', 1-imidazolyl or 1-(1, 2, 4-triazolyl);
lower alkyl, substituted or unsubstitued phenyl, or substituted or unsubstituted phenyl lower alkyl, wherein the substituents are 1 or 2 halogen atoms;
R" and R"' are each loweralkyl, which can bethesame or different;
X is halogen, lower alkoxy, or tower alkyl;
Y is N or CH; and
the pharmaceutically acceptable acid addition salts thereof;
to processes for the preparation thereof and to pharmaceutical compositions containing the compounds. The compounds are useful as antifungal agents.
本发明涉及通式如下的新型化合物
其中 n 为 0 或 1、
A 是 X-取代的苯基或 X-取代的噻吩基(苯基和噻吩基含有 1 2 个或 3 个取代基 X),或者,如果 n 为 1,A 也可以是 OR'、SR'、1-咪唑基或 1-(1,2,4-三唑基);
低级烷基、取代或未取代的苯基,或取代或未取代的苯基低级烷基,其中取代基为 1 或 2 个卤素原子;
R" 和 R"' 各为低级烷基,可以是相同的,也可以是不同的;
X 是卤素、低级烷氧基或塔烷基;
Y 是 N 或 CH;以及
其药学上可接受的酸加成盐;
其制备工艺和含有这些化合物的药物组合物。这些化合物可用作抗真菌剂。