SYNTHESIS OF 2-AMINO- AND 2-HYDRAZINO-SUBSTITUTED 5-NITRO-4,6-DIPHENYLPYRIMIDINES

Authors

  • В. Ф. Седова Novosibirsk N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090
  • O. П. Шкурко Novosibirsk N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090
  • C. А. Нехорошев Novosibirsk N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090

Keywords:

aminopyrimidines, hydrazinopyrimidines, nitropyrimidines, chloropyrimidines, nucleophilic substitution, mass spectrometry

Abstract

Nitrogen-containing derivatives of 5-nitro-4,6-diphenylpyrimidine have been synthesized by the reaction of 2-chloro-5-nitro-4,6-diphenylpyrimidine with amines or of 2-hydrazino-5-nitro-4,6-diphenylpyrimidine with carbonyl or β-dicarbonyl compounds. Their structures were confirmed by data of IR spectroscopy and mass spectrometry.

How to Cite
Sedova, V. F.; Shkurko, O. P.; Nekhoroshev, S. A. Chem. Heterocycl. Compd. 2002, 38, 564. [Khim. Geterotsikl. Soedin. 2002, 647.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1019561229703

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Published

2002-05-25

Issue

No. 5 (2002)

Section

Original Papers