Heterocyclization of N-propionylaminoindoline

Authors

  • В. П. Жестков All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • В. Н. Баринова All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • Ю. Н. Портнов All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • А. И. Чернышев All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450

Abstract

Treatment of N-propionylaminoindoline with a solution of phosgene in benzene gives the 1-[(indolin-1-yl)imino]propyl ester of 7-(1-cyanoethyl)indoline-1-carboxylic acid. The structure of the compound was proved using 1H and 13C NMR spectroscopy.

How to Cite
Zhestkov, V. P.; Barinova, V. N.; Portnov, Yu. N.; Chernyshev, A. I. Chem. Heterocycl. Compd. 1995, 31, 144. [Khim. Geterotsikl. Soedin. 1995, 168.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169668

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Published

1995-02-25

Issue

No. 2 (1995)

Section

Original Papers