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Chemistry of Heterocyclic Compounds

, Volume 9, Issue 4, pp 518–520 | Cite as

Cyanoethylation of 4-amino-1,2,4-triazolidine-3,5-dithione

  • A. D. Sinegibskaya
  • E. G. Kovalev
  • I. Ya. Postovskii
Article
  • 30 Downloads

Abstract

The cyanoethylation of 4-amino-1,2,4-triazolidine-3,5-dithione was studied. One cyanoethyl group adds to the nitrogen atom, while the other adds to the sulfur atom of the thioamide groupings. The mechanism of the reaction, which was confirmed by quantum-chemical calculations, was examined.

Keywords

Nitrogen Sulfur Organic Chemistry Nitrogen Atom Sulfur Atom 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

  1. 1.
    I. L. Shegal and I. Ya. Postovskii, Khim. GeterotsikI. Soedin., 443 (1965).Google Scholar
  2. 2.
    E. G. Kovalev and I. Ya. Postovskii, Khim Geterotsikl. Soedin., 1138 (1970).Google Scholar
  3. 3.
    Jo Sandström, Acta Chem. Scand., 15, 1295 (1961).Google Scholar

Copyright information

© Consultants Bureau 1975

Authors and Affiliations

  • A. D. Sinegibskaya
    • 1
  • E. G. Kovalev
    • 1
  • I. Ya. Postovskii
    • 1
  1. 1.S. M. Kirov Ural Polytechnic InstituteSverdlovsk

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