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2000
Volume 17, Issue 7
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

In the current study, a green, one-pot, three-component reaction was performed to prepare novel N-substituted 5-amino-1,3,4-thiadiazole derivatives. The thiadiazoles were obtained from the reaction of a ketene S,S-acetal of Meldrum’s acid or barbituric acid (as key intermediates), hydrazine, and isothiocyanate. The key advantages of this manner include environmentally safe reactions, high yield, appropriate reaction time, simple reaction conditions, and use of a green reaction solvent. The structure of thiadiazoles was determined based on the spectroscopic data.

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/content/journals/loc/10.2174/1570178616666190926105533
2020-07-01
2025-12-05
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