SYNTHESIS OF PYRROLO[<i>a</i>]- AND PYRROLO[<i>c</i>]PHENANTHRIDINE DERIVATIVES AND INDOLINYL AND INDOLYL-SUBSTITUTED 6-PHENANTHRIDINES

Authors

  • Е. П. Баберкина Russian University of Chemical Technology, Moscow 125190
  • В. Н. Буянов Russian University of Chemical Technology, Moscow 125190
  • М. Е. Жукова Russian University of Chemical Technology, Moscow 125190
  • А. Е. Щекотихин Russian University of Chemical Technology, Moscow 125190
  • В. Е. Жигачев Russian University of Chemical Technology, Moscow 125190
  • Н. Н. Суворов Russian University of Chemical Technology, Moscow 125190

Keywords:

6-(1-acetyl-5-indolinyl)phenanthridine, 6-(1-indolyl)phenanthridine, 6-methyl-1H-pyrrolo[2,3-a]- and 4-methyl-3H-pyrrolo[3,2-c]phenanthridinium Mannich bases

Abstract

The corresponding Mannich bases have been synthesized by the aminomethylation of 6-methyl-1H-pyrrolo[2,3-a]- and 4-methyl-3H-pyrrolo[3,2-c]phenanthridinium iodides. The interaction of 6-chloro-phenanthridine with indoline and with 5-amino-N-acetylindoline gave the corresponding derivatives of phenanthridine. 6-(1-Indolyl)phenanthridine has been obtained by the dehydrogenation of 6‑(1‑indolinyl)phenanthridine with manganese dioxide.

How to Cite
Baberkina, E. P.; Buyanov, V. N.; Zhukova, M. E.; Shchekotikhin, A. E.; Zhigachev, V. E.; Suvorov, N. N. Chem. Heterocycl. Compd. 2001, 37, 1234. [Khim. Geterotsikl. Soedin. 2001, 1350.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1013897410464

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Published

2001-10-25

Issue

No. 10 (2001)

Section

Original Papers