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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

The synthesis and chemistry of 2-Methylpyrimidine-4,6-dithiol and some related compounds

DT Hurst

Australian Journal of Chemistry 36(7) 1477 - 1482
Published: 1983

Abstract

2-Methylpyrimidine-4,6-dithiol has been synthesized and has been converted into 2-methyl-6- methylthiopyrimidine-4-thiol, 4,6-bismethylthiopyrimidine and 6,6'-dithiobis(2-methylpyrimidine-4- thiol). Oxidation of 4,6-bismethylthio-2-methylpyrimidine with 1, 2, 3 and 4 equiv. of m-chloroper- benzoic acid has been shown to result in the formation of the easily isolable methylsulfinyl(methylthio)-, bis(dimethylsulfinyl)-, methylsulfinyl(methylsulfonyl)- and bismethylsulfonyl-pyrimidine, respectively. Some further reactions of the above compounds are described and the synthesis of some other pyrimidines having sulfur-containing substituents is also described.

https://doi.org/10.1071/CH9831477

© CSIRO 1983

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