Issue 4, 1997

A new route to the antitumour drug temozolomide, but not thiotemozolomide

Abstract

Interaction of 5-aminoimidazole-4-carboxamide with alkyl isocyanates yields N-substituted 1-carbamoylimidazoles which can be cyclised to imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-ones, including temozolomide 3a, on nitrosation; a similar reaction with methyl isothiocyanate, followed by nitrosation, affords the nitrosomethylamino derivative 11 of a new ring-system, imidazo[1,5-b][1,2,4]thiadiazole.

Article information

Article type
Paper

Chem. Commun., 1997, 363-364

A new route to the antitumour drug temozolomide, but not thiotemozolomide

Y. Wang, P. R. Lowe, W. T. Thomson, J. Clark and M. F. G. Stevens, Chem. Commun., 1997, 363 DOI: 10.1039/A606159A

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