Skip to main content
Log in

N-Amination of Unsymmetrically Substituted Pyrimidines. Synthesis of Isomeric N-Aminopyrimidones

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

N-Amination of 6-amino-2-methyl-4-pyrimidone with O-(mesitylenesulfonyl)hydroxylamine leads to the 3-amino derivative. The isomeric 1,6-diamino-2-methyl-4-pyrimidone was obtained by the N-amination of the O-benzoyl derivative of the initial pyrimidone and removal of the benzoyl protection.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. Y. Tamura, J. Minamikawa, and M. Ikeda, Synthesis, 1 (1977).

  2. A. Yu. Ivanov, V. P. Tsyrenov, N. G. Antonov, P. S. Lobanov, and A. A. Potekhin, Khim. Geterotsikl. Soedin., 807 (2002).

  3. Z. Foldi, G. V. Fodar, I. Demjen, H. Szeker, and J. Halmos, Ber., 75, 755 (1942).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bodyagin, M.B., Ivanov, A.Y., Wurst, K. et al. N-Amination of Unsymmetrically Substituted Pyrimidines. Synthesis of Isomeric N-Aminopyrimidones. Chemistry of Heterocyclic Compounds 39, 195–199 (2003). https://doi.org/10.1023/A:1023716424186

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1023716424186

Navigation