SYNTHESIS OF SUBSTITUTED PYRROLO[3,2-<i>f</i>]QUINOLINES

Authors

  • C. А. Ямашкин M. E. Evsev'ev Mordovian State Pedagogical Institute, Saransk 430007
  • Н. Я. Кучеренко M. E. Evsev'ev Mordovian State Pedagogical Institute, Saransk 430007
  • М. А. Юpoвская M. V. Lomonosov Moscow State University, Moscow 119899

Abstract

Reactions of 2,3,6-trimethyl- and 2,6-dimethyl-6-methoxy-5-aminoindoles with 1,3-dicarbonyl compounds represent a convenient route for obtaining substituted pyrrolo[3,2-f]quinolines, even though the presence of a methoxy group on the benzene ring sometimes lowers the reactivity of the amine, thus increasing the required reaction time and reducing the yield.

How to Cite
Yamashkin, S. A.; Kucherenko, N. Y.; Yurovskaya, M. A. Chem. Heterocycl. Compd. 1997, 33, 942. [Khim. Geterotsikl. Soedin. 1997, 1080.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253166 

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Published

1997-08-25

Issue

No. 8 (1997)

Section

Original Papers