The reactions of 5-merkapto-3,4-disubstituted-1,2,4-triazoles with ethyl chloroacetate have been investigated. It has been shown that mercapto group reacted and S-substituted derivatives were formed. On the next step hydrazinolysis by 85% hydrazine hydrate was carried out and on the base of obtained hydrazides thiosemicarbazides were synthesized. Further by means of intermolecular cyclization bis-1,2,4-triazoles were obtained, structure of heterocyclic rings were connected by thio-methyl bridge.
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Organic Chemistry
, 2025, Issue 1, pp. 1–10
ISSN Online: 0000-0000
DOI:
10.xxxx/example-doi