G. A. Mokrushina, S. Kotovskaya, V. I. Il'enko
Mar 1, 1988
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Journal
Pharmaceutical Chemistry Journal
Abstract
We have previously reported [4] that in 2-hydrazinobenzimidazoles, the greatest antiviral activity is shown by compounds bearing a carboxy or ethoxycarbonyl group in the 5-position. Continuing work on the synthesis and examination of the antiviral activity of benzimidazoles, we have synthesized some benzimidazole-5-carboxamides substituted in the 2-position with chloro-, hydrazine-, and isopropylidene (and isobutylidene)hydrazino-groups (III-XIX).