Abstract
Alkylation of 2-phenylamino-4-methylthiazole with substituted phenacyl bromides led to the synthesis of hydrobromides of 2-phenylimino-3-(p-R-phenacyl)-4-methylthiazoles. It was shown that, depending on the conditions of the cyclization of the last, 3-methyl-6-aryl-7-phenyl- or 3-methyl-5-aroyl-6-alkyl-7-phenylimidazo[2,1-b]thiazolium bromides can be synthesized. The spectral characteristics of the compounds synthesized were studied.
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