REACTION OF 4,5-DINITROIMIDAZOLE WITH ETHYLENEDIAMINE AND SOME TRANSFORMATIONS OF THE OBTAINED 5-(2-AMINOETHYLAMINO)-4-NITRO-1H-IMIDAZOLE

Authors

  • О. С. Ельцов Ural State Technical University, Ekaterinburg 620002
  • В. С. Мокрушин Ural State Technical University, Ekaterinburg 620002

Keywords:

benzothiazole, bifunctional amines, dinitroimidazole, imidazolylthioureides, nitro group, ethylenediamine, acylation

Abstract

The nitro group at position 5 in 4,5-dinitroimidazole was substituted by reaction with ethylenediamine with the formation of 5-(2-aminoethylamino)-4-nitro-1H-imidazole. The acylation of the compound was studied; a new bicyclic derivative of imidazole containing a benzothiazole fragment was obtained.

How to Cite
El'tsov, O. S.; Mokrushin, V. S. Chem. Heterocycl. Compd. 2002, 38, 1331. [Khim. Geterotsikl. Soedin. 2002, 1513.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1022122208213

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Published

2002-11-25

Issue

No. 11 (2002)

Section

Original Papers