PHENYL-ACETONITRILE DERIVATIVE, MANUFACTURE AND MEDICINE FORTREATING CARDIAC AND CIRCULATORY DISEASES

The present invention provides phenylacetonitrile derivatives of the general formula: (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 methy...

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Hauptverfasser: KURAUSU SHIYUTORAIN, BUORUFUGANGU KANPE, BUORUFUGANGU BARUCHIYU, BERUNTO MIYURAA BETSUKUMAN, HERUBERUTO RAINERUTO
Format: Patent
Sprache:eng
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Zusammenfassung:The present invention provides phenylacetonitrile derivatives of the general formula: (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: 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: 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.