864629-15-2Relevant articles and documents
Synthesis and antimicrobial activity of 1,3,5-thiadiazines and their isomerism into 1,3,5-triazines
Deohate, Pradip P.,Berad
, p. 638 - 642 (2007/10/03)
A series of 2,6-diphenylimino-4-(substituted)-benzylidene amino-1,3,5-thiadiazines 4a-g have been obtained by the basification of their hydrochlorides 3a-g, which are prepared by interaction of N-phenyl isocyanodichloride and 1-(substituted)-benzylidene amidino-3-phenyl thiocarbamides 2a-g. The latter have been synthesized by the condensation of 1-amidino-3-phenyl thiocarbamide 1 and different aliphatic and aromatic aldehydes. Compounds 4a-g on acylation afford monoacetyl derivatives 5a-g, on reaction with sodium nitrite in acidic medium afforded mononitroso derivatives 6a-g, and on boiling with 5% aqueous ethanolic (1:1) sodium hydroxide solution isomerize into corresponding 1-phenyl-2-phenylimino-4-(substituted)-benzylidene amino-6-thio-1,3,5-triazines 7a-g. The title compounds have been assayed for their antimicrobial activity against gram-positive as well as gram-negative microorganisms.
