REACTIONS OF 2,3-DIOXOPYRROLO[2,1-<i>a</i>]ISOQUINOLINES WITH AMMONIA AND ALIPHATIC AMINES

Authors

  • A. G. Mikhailovskii Perm State Pharmacological Academy, Perm 614990
  • N. N. Polygalova Perm State Pharmaceutical Academy, Perm 614990
  • T. S. Turova Perm State Pharmaceutical Academy, Perm 614990
  • G. A. Lobashova Perm State Pharmaceutical Academy, Perm 614990
  • M. I. Vahrin Perm State Pharmaceutical Academy, Perm 614990

Keywords:

amides of (3,3-dialkylisoquinolinidene-1)pyruvic and 2-oxobutandioic acids, ammonia, 5,5-dialkyl-2,3-dioxopyrrolo[2,1-a]isoquinolines, methylamine, ethylamine

Abstract

2,3-Dioxopyrrolo[2,1-a]isoquinolines, with either a tertiary amide substituent at position 1 or no substituent, react with ammonia and aliphatic amines with ring opening to form the corresponding enamino keto amides.

How to Cite
Mikhailovskii, A. G.; Polygalova, N. N.; Turova, T. S.; Lobashova, G. A.; Vahrin, M. I. Chem. Heterocycl. Compd. 2004, 40, 1174. [Khim. Geterotsikl. Soedin. 2004, 1357.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000048291.71402.3b

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Published

2004-09-25

Issue

No. 9 (2004)

Section

Original Papers