Reactions of α-Polyhalo Ketone Tosylhydrazones with Sulfide Ion and Primary Amines. Cyclization to 1,2,3-Thiadiazoles and 1,2,3-Triazoles

Abstract

Trichloroacetaldehyde tosylhydrazone acts as an excellent precursor of diazodithioacetate which is generated by treatment of the hydrazone with sulfide ion. This spontaneously cyclizes it to 5-mercapto-1,2,3-thiadiazole. The precursor also gives a 5-amino-1,2,3-triazole on reaction with an amine. α,α-Dichloro ketone tosylhydrazones similarly cyclize to give 1,2,3-thiadiazoles and 1,2,3-triazoles.