Potassium β acyl dithio-carbazinates (4a-r) were obtained by condensation of acid hydrazides (3a-r) with carbon disulphide in ethanolic potassium hydroxide. On heating (4a-r) and isonicotinic acid hydrazide (INH) 4-(N-pyridy carboxamide)-5-mercapto-3-substituted-1,2,4-triazoles (5a-r) were obtained. These compounds were screened for antimicrobial activity.
|Number of pages||4|
|Journal||Indian Journal of Heterocyclic Chemistry|
|Publication status||Published - 1996|
Udupi, R. H., & Bhat, A. R. (1996). Synthesis of 4-(N-pyridyl carboxamido)-5-mercapto-3-substituted-1.2.4-triazoles for possible antitubercular activity. Indian Journal of Heterocyclic Chemistry, 6(1), 41-44. https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030365481&partnerID=40&md5=d022cd2d98a5cf65c482f5b5fc000429