Synthesis of 2-anilino-7-hydroxy-6H-1,3,4-thiadiazepines by the reaction of 1-acyl-2-phenylacetylenes with 4-phenylthiosemicarbazides

Authors

  • А. C. Нахманович Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk
  • T. E. Глoтова Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk

Abstract

2-Anilino-7-hydroxy-7-methyl(phenyl, thienyl-2)-6H-1,3,4-thiadiazepines have been obtained in good yield by the reaction of 4-phenylthiosemicarbazides with 1-acyl-2-phenylacetylenes using glacial acetic acid as condensing agent.

How to Cite
Nakhmanovich, A. S.; Glotova, G. E. Chem. Heterocycl. Compd. 1996, 32, 119. [Khim. Geterotsikl. Soedin. 1996, 130.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169367

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Published

1996-01-25

Issue

No. 1 (1996)

Section

Original Papers