Novel Approach for the Synthesis of 2, 5-disubstituted 1, 3, 4-thiadiazoles from Benzothiohydrazides and Ethylbenzimidate

Abstract

INTRODUCTION: In the current study, a simple and reliable technique for the synthesis of 2,5-disubstituted 1,3,4-thiadiazoles from ethylbenzimidate and benzothiohydrazides were devised. METHOD: This protocol goes via a base-mediated nucleophilic addition elimination process, followed by intramolecular rearrangement RESULT: Our method utilizes commonly accessible and non-toxic substrates and a simple workup procedure to produce high to exceptional yields (70-91%) of 2,5-diphenyl 1,3,4-thiadiazoles derivatives with a wide range of substitutions. CONCLUSION: we present a simple procedure for the synthesis of 1, 3, 4-thiadiazole using ethylbenzimidate and benzothiohydrazides in the presence of Et3N in DMSO solvent as affordable and easily accessible starting materials to create derivatives under ambient conditions.