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.
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