Synthesis and in vitro study of [1,3,4]thiadiazol-2yl-3,3a,5,6-tetrahydro-2H-pyrazolo[3,4-d]thiazoles as antimicrobial agents

A variety of 3,5-diphenyl-6-(5-p-toly1-[1,3,4] thiadiazol-2yl)-3,3a,5,6 tetrahydro-2H pyrazolo[3,4-d]thiazole 6ag were synthesized by the reaction of chalcone derivatives of [1,3,4] thiadiazol-2-yl)-thiazolidin-4-one 5a–g with hydrazine hydrate. The chemical structures of these compounds were confirmed by IR, NMR (1H & 13C) and mass spectral studies. Synthesized compounds 6a–g were evaluated for their antimicrobial and anti-tubercular activities. Some of the compounds exhibited well antimicrobial and anti-tubercular activities compared to the standard drugs.