Synthesis of S-((Arylamino)formimidoyl)-2-thiobarbituric Acid Hydrochloride Antituberculous Agents

Abstract

Various S -((arylamino)formimidoyl)-2-thlobarbituric acid hydrochlorides have been synthesized by the condensation of corresponding arylcyanamides with 2-thlobarbituric acid and 1-substituted-2-thlobarbituric acids. Precursors required In these syntheses were prepared by already known methods. © 1985, American Chemical Society. All rights reserved.