

Author: Dzvinchuk I. Lozinskii M.
Publisher: Springer Publishing Company
ISSN: 0009-3122
Source: Chemistry of Heterocyclic Compounds, Vol.41, Iss.11, 2005-11, pp. : 1419-1423
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Abstract
Cyanoethylhydrazones of 2-aroylmethyl-1H-benzimidazoles undergo recyclization on reaction with trifluoroacetyl anhydride to give 3-aryl-1-cyanoethyl-5-(2-trfluoroacetaminoanilino)pyrazoles. The recyclization products may be cyclized with closing of the benzimidazole ring in two ways: with formation of 1-(5-pyrazolyl)benzimidazoles or 5,6-dihydroderivatives of a new polyheterocyclic system — pyrazolo[5′,1′: 2,3]pyrimido[1,6-a]benzimidazole.
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