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Heterocyclization of compounds containing diazo and cyano groups. 2. Synthesis and recyclization of 4-substituted 5-amino-1,2,3-thiadiazoles (in Russian)

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00519542· OSTI ID:6164307

The reaction of carbonyl derivatives of diazoacetonitrile with hydrogen sulfide in the presence of triethylamine yields 4-substituted 5-amino-1,2,3-triadiazoles. Under analogous conditions, hydrogen selenide and ethyl mercaptan reduce the starting diazo compounds to hydrazones. Thiadiazoles are recyclized to 4-substituted 5-mercapto-1,2,3-triazoles by the action of bases.

Research Organization:
S. M. Kirov Urals Polytechnical Institute, Sverdlovsk, USSR
OSTI ID:
6164307
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 22:5; ISSN CHCCA
Country of Publication:
United States
Language:
Russian

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