SYNTHESIS AND PROPERTIES OF TRIETHYLAMMONIUM 4-ARYL(HETARYL)-3,5-DICYANO-6-OXO-1,4,5,6-TETRAHYDROPYRIDINE-2-SELENOLATES

Authors

  • К. А. Фролов "ChemEx" Laboratory, Vladimir Dal' East-Ukrainian National University
  • В. В. Доценко "ChemEx" Laboratory, Vladimir Dal' East-Ukrainian National University
  • С. Г. Кривоколыско "ChemEx" Laboratory, Vladimir Dal' East-Ukrainian National University
  • В. П. Литвинов N. D. Zelinsky Institute of Organic Chemistry

DOI:

https://doi.org/10.1007/1233

Keywords:

1-cyanoacetyl-3, 5-dimethylpyrazole, cyanoselenoacetamide, (hetero)aromatic aldehydes, tetrahydropyridine-2-selenolates, heterocyclization

Abstract

The reaction of (hetero)aromatic aldehydes, cyanoselenoacetamide, and 1-(cyanoacetyl)-3,5-dimethyl-pyrazole in the presence of triethylamine gives a mixture of the cis and trans diastereomers of triethylammonium 4-aryl(hetaryl)-3,5-dicyano-6-oxo-1,4,5,6-tetrahydropyridine-2-selenolates. The selenolates obtained react with alkyl halides to form the corresponding selenides.

Authors: K. A. Frolov, V. V. Dotsenko, S. G. Krivokolysko, and V. P. Litvinov.

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (3), pp 442-447

http://link.springer.com/article/10.1007/s10593-012-1012-4

Published

2013-11-25

Issue

Section

Original Papers