RECYCLIZATION REACTIONS OF 2-(1-BENZOYLPYRROLIDIN-2-YLIDENE)MALONONITRILE

Authors

  • К. В. Швиденко Institute of Organic Chemistry, National Academy of Sciences of Ukraine
  • К. Г. Назаренко Institute of Organic Chemistry, National Academy of Sciences of Ukraine
  • Т. И. Швиденко National Agricultural University of Ukraine
  • А. А. Толмачев Research and Development Center for Chemistry and Biology, Kiev T. Shevchenko National University

DOI:

https://doi.org/10.1007/2780

Keywords:

ω-aminoalkylheterocycles, binucleophiles, cyclic enamines, recyclization

Abstract

Acylation of pyrrolidin-2-ylidenemalononitrile with benzoyl chloride leads to the formation of 2-(1-benzoylpyrrolidin-2-ylidene)malononitrile. The obtained product was used as starting material in the synthesis of γ‑aminopropylpyrazoles and pyrimidines.

How to Cite
Shvidenko, K. V.; Nazarenko, K. G.; Shvidenko, T. I.; Tolmachev, A. A. Chem. Heterocycl. Compd. 2010, 46, 56. [Khim. Geterotsikl. Soedin. 2010, 67.]

For this article in the English edition see DOI 10.1007/s10593-010-0469-2

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Published

2015-11-25

Issue

No. 1 (2010)

Section

Original Papers