SYNTHESIS OF FUNCTIONALLY SUBSTITUTED PYRROLO[3,2-<i>g</i>]QUINOLINES FROM 6-AMINO-7-METHOXY-1,2,3-TRIMETHYLINDOLE

Authors

  • С. А. Ямашкин Mordovian State Pedagogical Institute, Saransk 430007
  • Е. А. Орешкина Mordovian State Pedagogical Institute, Saransk 430007
  • И. С. Романова Mordovian State Pedagogical Institute, Saransk 430007
  • М. А. Юровская M. I. Lomonosov Moscow State University, Moscow 11989

DOI:

https://doi.org/10.1007/8169

Keywords:

6-amino-7-methoxy-1, 2, 3-trimethylindole, acetylacetone, acetoacetic ester, dibenzoylmethane, functionally substituted pyrrolo[3, 2-g]quinolines, trifluoroacetoacetic ester.

Abstract

The comparative reactivities of  6-amino-1,2,3-trimethyl- and 6-amino-7-methoxy-2,3-dimethylindoles with acetylacetone, dibenzoylmethane, and with aceto- and trifluoroacetoacetic esters have been studied. Methods have been developed for the preparation  of some functionally substituted pyrrolo-[3,2-g]quinolines.

How to Cite
Yamashkin, S. A.; Oreshkina, E. A.; Romanova, I. S.; Yurovskaya, M. A.  Chem. Heterocycl. Compd. 2005, 41, 1280. [Khim. Geterotsikl. Soedin. 2005, 1529.]

For this article in the English edition, see DOI 10.1007/s10593-005-0314-1


Downloads

Published

2023-10-19

Issue

No. 10 (2005)

Section

Original Papers