SYNTHESIS OF N,N'-ALKYLATED TETRAHYDROQUINOXALINES BY THE REACTION OF 4-BROMO-5-NITROPHTHALONITRILE WITH SECONDARY DIAMINES

Authors

  • И. Г. Абрамов Yaroslavl State Technical University, Yaroslavl 150023
  • А. B. Смирнов Yaroslavl State Technical University, Yaroslavl 150023
  • M. Б. Абрамова Yaroslavl State Technical University, Yaroslavl 150023
  • C. А. Ивановский Yaroslavl State Technical University, Yaroslavl 150023
  • M. C. Белышева Yaroslavl State Technical University, Yaroslavl 150023

Keywords:

bifunctional nucleophiles, 4-bromo-5-nitrophthalonitrile, tetrahydroquinoxaline, nucleophilic substitution

Abstract

The reaction of 4-bromo-5-nitrophthalonitrile with aliphatic secondary diamines to give dicyano tetrahydroquinoxalines alkylated on the nitrogen atoms has been investigated for the first time. The latter can be used to prepare imides, phthalocyanines, hexazocyclanes, and other compounds containing isoindoline fragment.

How to Cite
Abramov, I. G.; Smirnov, A. V.; Abramova, M. B.; Ivanovskii, S. A.; Belysheva, M. S. Chem. Heterocycl. Compd. 2002, 38, 576. [Khim. Geterotsikl. Soedin. 2002, 660.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1019565330611

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Published

2002-05-25

Issue

No. 5 (2002)

Section

Original Papers