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PHENYL ACETONITRICE DERIVATIVES CONTAINING A NITROOXY ONO2 SUBSTITUENT

机译:含有硝基氧ONO2取代基的苯乙炔衍生物

摘要

The present invention provides phenylacetonitrile derivatives of the general formula: IMAGE (I) wherein R1, R2, R3, R4 and R5, which can be the same or different, are hydrogen or haolgen atoms or alkyl, alkoxy, nitro, amino or acylamino radicals and two adjacent substituents can together also form a methylenedioxy or ethylenedioxy radical, A is a radical of the general formula: IMAGE in which R6 is a straight-chained, cyclic or branched, saturated or unsaturated alkyl radical containing 2 to 12 carbon atoms, R7 is a hydrogen atom or a straight-chained or branched, saturated alkyl radical containing up to 6 carbon atoms, m and n, which can be the same or different, are 2 or 3, p is 1 or 2 and X is a straight-chained, cyclic or branched alkyl radical containing 2 to 10 carbon atoms which is optionally substituted by an amino group or is a grouping of the general formula: IMAGE wherein Y and Z, which can be the same or different, are straight-chained or branched alkyl radicals containing up to 8 carbon atoms or cycloalkyl, alkylcycloalkyl or cycloalkylalkyl radicals, in which these radicals are optionally interrupted by an oxygen or sulphur atom, and one of the groups Z in general formula II can also be a hydrogen atom or both Z groups are joined to form a ring containing 4 to 6 carbon atoms which is optionally interrupted by a further nitrogen atom which can be substituted by alkyl or alkanoyl, the -O-NO2 groups being substituents of Y as well as of Z; as well as the salts thereof with physiologically acceptable acids. The present invention also provides processes for the preparation of these compounds and pharmaceutical compositions containing them.
机译:本发明提供通式:(I)的苯乙腈衍生物,其中R 1,R 2,R 3,R 4和R 5可以相同或不同,是氢或卤素原子或烷基,烷氧基,硝基,氨基或烷基。酰基氨基和两个相邻的取代基也可以一起形成亚甲基二氧基或亚乙基二氧基。A是通式的基团:,其中R6是含2至12的直链,环状或支链的饱和或不饱和烷基碳原子,R7是氢原子或直链或支链的饱和烷基,最多可包含6个碳原子,m和n可以相同或不同,为2或3,p为1或2和X是含有2-10个碳原子的直链,环状或支链烷基,其可任选地被氨基取代或为通式:的基团,其中Y和Z可以相同或不同,是直链或支链的烷基包含最多8个碳原子或环烷基,烷基环烷基或环烷基烷基的基团,其中这些基团可选地被氧或硫原子间断,并且通式II中的基团Z也可以是氢原子或两个Z基团是连接形成含4至6个碳原子的环,该环任选地被可被烷基或链烷酰基取代的另外的氮原子所中断,-O-NO 2基团是Y以及Z的取代基;以及它们与生理上可接受的酸形成的盐。本发明还提供了制备这些化合物的方法和包含它们的药物组合物。

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