N-SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR SALTS, METHOD OF PREPARATION THEREOF, INTERMEDIATE COMPOUNDS AND PHARMACEUTICAL COMPOSITION WITH ANGIOTENSINE II ANTAGONIST ACTIVITY Russian patent published in 1998 - IPC

Abstract RU 2107062 C1

FIELD: preparation of biologically active substances. SUBSTANCE: compounds of invention have general formula where R1 and R2, the same or different, are hydrogen, C1-C6-alkyl, (C1-C4)-alkoxyl, amino, aminomethyl, carboxyl, C1-C4-alkoxycarbonyl, cyano, tetrazolyl, methyltetrazolyl, methylsulfonylamino, trifluoromethylsulfonylamino, trifluoromethylsulfonylaminomethyl, N-cyanoacetamido, N- hydroxyacetamido, N-(4-carboxy-1,3-thizol-2-yl)acetamido, ureido, 2- cyanoguanidinocarbonyl, or 2-cyanoguanidinomethyl, provided that at least one R1 or R2 is not hydrogen; R3 is hydrogen, C1-C6-alkyl that may be substituted by one or more halogen atoms, C2-C6-alkenyl, C3-C7- cycloalkyl, phenyl, phenyl-C1-C3-alkyl, phenyl-C2-C3-alkenyl (indicated phenyl groups being optionally substituted by one ore more halogen atoms), C1-C4-alkyl, halo-C1-C4-alkyl, polyhalo-C1-C4-alkyl, hydroxyl, or C1-C4-alkoxyl; R4 is C1-C4-alkyl optionally substituted by one or more halogen atoms; R5-cycloalkyl or C3-C7-cycloalkylmethyl optionally substituted by one or more halogen atoms; each of R4 and R5 groups may also be cyclopropyl; X is oxygen or sulfur; z= t=0 or one of them is 0 and other 1. EFFECT: provided new useful biologically active substances. 10 cl, 1 tbl

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RU 2 107 062 C1

Authors

P'Er Perro[Fr]

Klod Mjuno[Fr]

Ivett Mjuno[Fr]

Dates

1998-03-20Published

1992-09-09Filed