Synthesis and heterocyclization of N-phenylaminolactams

Authors

  • B. П. Жестков All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • В. В. Дружинина All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • А. B. Рудницких All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450

Abstract

Intramolecular alkylation of N-phenylhydrazides of δ-chlorovaleric and ɛ-chlorocaproic acids was used to prepare the corresponding N-phenylaminolactams. Their reaction with phosphoryl chloride formed the corresponding condensed tricyclic systems of tetrahydro-α-carbolines and azepino[2,3-b]indole. 

How to Cite
Zhestkov, V. P.; Druzhinina, V. V.; Rudnitskikh, A. V. Chem. Heterocycl. Compd. 1995, 31, 1307. [Khim. Geterotsikl. Soedin. 1995, 1507.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01168625

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Published

1995-11-25

Issue

No. 11 (1995)

Section

Original Papers