Reactions of imidazolethiones with phenylcyanoacetylene

Autor: Skvortsova, G. G., Abramova, N. D., Mal'kina, A. G., Skvortsov, Yu. M., Trzhtsinskaya, B. V., Albanov, A. I.
Zdroj: Chemistry of Heterocyclic Compounds; July 1982, Vol. 18 Issue: 7 p736-739, 4p
Abstrakt: The reaction of phenylcyanoacetylene with imidazolethiones was studied. It is shown that in the presence of 5–10% KOH the addition of phenylcyanoacetylene is accompanied by intramolecular cyclization with the formation of imidazo-1,3-thiazines. An increase in the amount of catalyst to 20% leads to cleavage of the thiazine ring at the C-S bond and the formation of the corresponding acrylonitrile derivatives. Products of addition of 2 moles of phenylcyanoacetylene were obtained.
Databáze: Supplemental Index