Methylation of heterocyclic compounds containing NH, SH and/or OH groups by means of N,N-dimethylformamide dimethyl acetal
- 1 January 1981
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 34 (8) , 1729-1738
- https://doi.org/10.1071/ch9811729
Abstract
Methylations of heterocyclic systems, such as benzimidazole, naphth[2,3-c]imidazole, imidazo[4,5-c]-pyridine, purine, pyridine, pyrimidine, pyridazine and s-triazolo[4,3-b]pyridazine, which bore SH, NH and/or OH groups, were carried out with dimethylformamide dimethyl acetal to give the corresponding S-, N- and/or O-methyl derivatives in high yields. Selective methylation of some compounds containing both SH and NH groups took place to give first the S-methyl and subsequently the S,N-dimethyl derivatives. No side reactions, such as C-methylation, were observed.Keywords
This publication has 2 references indexed in Scilit:
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- The Synthesis and Properties of 6-Chloropurine and Purine1Journal of the American Chemical Society, 1954