2,N-dicyanoacetamidine in the regioselective synthesis of pyrido[2,3-<i>d</i>]uracils

Authors

  • B. Л. Иванов N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • B. А. Артемов N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • А. М. Шестопалoв N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • B. П. Литвинов N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow

Abstract

A new regioselective method of synthesizing functionally substituted pyrido[2,3-d]uracils from 2,N-dicyanoacetamidine is proposed. 3-Cyanopyridinecyanoimidines and 4-amino-2-bromopyrido[2,3-d]pyrimidine hydrobromides were obtained as intermediate compounds. The structures of the compounds obtained were established by data of elemental analysis, NMR, IR, and mass spectra.

How to Cite
Ivanov, V. L.; Artemov, V. A.; Shestopalov, A. M.; Litvinov, V. P. Chem. Heterocycl. Compd. 1995, 31, 582. [Khim. Geterotsikl. Soedin. 1995, 659.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01166334

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Published

1995-05-25

Issue

No. 5 (1995)

Section

Original Papers