FIELD: chemistry.
SUBSTANCE: invention relates to novel antiviral active components which are substituted 2-aminomethyl-1-benzyl-1H-benzo[d]imidazoles of general formula 1 or pharmaceutically acceptable salts thereof, a pharmaceutical composition, antiviral medicinal agents, a method of preventing and treating viral diseases, especially those cause by hepatitis C virus (HCV). In general formula 1
, R1 denotes one or two substitutes of a cyclic system, including a hydrogen atom, C1-C3 alkyl, C1-C3 alkyloxy or a halogen atom; R2 denotes a hydrogen atom or C1-C3 alkyl; R3 and R4 denote identical substitutes of amine groups, including hydrogen, C1-C2 alkyl, C1-C3-alkanoy, optionally substituted furanoyl; optionally substituted or optionally annelated with a 5-6-member azaheterocyclic ring of phenyl; or R3 and R4 together with a nitrogen atom with which they are bonded form a morpholin4-yl, 4- (C1-C3 alkylsubstituted)-piperazin-1-yl, and R1 and R2 assume values given above, or piperidin-1-yl, provided that R1 assumes the value given above, R2 denotes C1-C3 alkyl, or provided that R1 denotes hydrogen or o-fluorine, R2 assumes the value given above.
EFFECT: improved method.
7 cl, 1 tbl, 4 ex
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