Chemistry of Heterocyclic Compounds

, Volume 48, Issue 11, pp 1696–1700

Facile synthesis of new (Z)-6-arylmethylidene-1,3,4-thiadiazin-5(6H)-one derivatives

Authors

    • Cairo University
  • F. M. Abdelrazek
    • Cairo University
  • A. Jaeger
    • Institute of Organic ChemistryTechnical University of Dresden
Article

DOI: 10.1007/s10593-013-1195-3

Cite this article as:
Metwally, N.H., Abdelrazek, F.M. & Jaeger, A. Chem Heterocycl Comp (2013) 48: 1696. doi:10.1007/s10593-013-1195-3

3-Aryl-2-sulfanylpropenoic acids reacted with acetohydrazonyl chlorides in refluxing absolute ethanol in the presence of equimolar amounts of triethylamine, forming (Z)-6-arylmethylidene-1,3,4-thiadiazin-5-one derivatives. X-ray study on the crystal of one of the obtained products was carried out.

Keywords

N'-arylacetonitrilimines (Z)-6-arylmethylidene-1,3,4-thiadiazin-5(6H)-one derivatives 3-aryl-2-sulfanylpropenoic acids

Copyright information

© Springer Science+Business Media New York 2013