Issue 0, 1974

Purine studies. Part XII. Derivatives resulting from acylation and subsequent ethylation of 4,5-diamino-6-methyl-2-methylthiopyrimidine

Abstract

The structures of the various products arising from acetylation of 4,5-diamino-6-methyl-2-methylthiopyrimidine have been identified by means of 1H n.m.r. and by their conversion into known compounds. Ethylation of the acetylated derivatives does not take place at the same exocyclic nitrogen atom in every case; the site of reaction is a reflection of the change in relative basicity of the 4- and 5-amino-groups which results from their acetylation.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1300-1303

Purine studies. Part XII. Derivatives resulting from acylation and subsequent ethylation of 4,5-diamino-6-methyl-2-methylthiopyrimidine

M. D. Fenn and J. H. Lister, J. Chem. Soc., Perkin Trans. 1, 1974, 1300 DOI: 10.1039/P19740001300

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements