FORMATION OF 3-ACYLAMINO-2-ARYLHYDRAZONO-3-CYANO-2,3-DIHYDRO-1<i>H</i>-INDOLES IN THE REACTION OF 2-ACYLAMINO-3,3-DICHLOROACRYLONITRILES WITH ARYLHYDRAZINES

Authors

  • С. А. Чумаченко Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine
  • О. В. Шаблыкин Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine
  • А. Н. Василенко Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine
  • Э. Б. Русанов Institute of Organic Chemistry, National Academy of Sciences of Ukraine
  • В. С. Броварец Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine

DOI:

https://doi.org/10.1007/1161

Keywords:

2-acylamino-3, 3-dichloroacrylonitrile, 2-aryl-4-cyano-5-(2-phenylhydrazino)-1, 3-oxazole, arylhydrazine, N-{[(2Z)-2-arylhydrazono-3-cyano]-2, 3-dihydro-1H-indol-3-yl}amides of carboxylic acids, heterocyclization

Abstract

The reaction of 2-acylamino-3,3-dichloroacrylonitriles with arylhydrazines in tetrahydrofuran upon heating was investigated. It led to previously unknown 3-acylamino-2-arylhydrazono-3-cyano-2,3-dihydro-1H-indoles.

Authors: S. A. Chumachenko, O. V. Shablykin, A. N. Vasilenko, E. B. Rusanov, and V. S. Brovarets.

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (6), pp 881-887

http://link.springer.com/article/10.1007/s10593-012-1070-7

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Published

2013-11-14

Issue

No. 6 (2012)

Section

Original Papers