New access to thiazolo[4,5-d]pyrimidine derivatives

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Abstract

4-Amino-5-bromo-2-substituted-aminopyrimidines are readily obtained from the newly prepared 5-bromo-2,4-dichloro-6-methylpyrimidine by sequential treatment with ethanolic ammonia and secondary amines. These compounds were successfully reacted with various isothiocyanates in the presence of sodamide in DMF to form the new thiazolo[4,5-d] pyrimidine derivatives.

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Bakavoli, M., Nikpour, M., & Rahimizadeh, M. (2006). New access to thiazolo[4,5-d]pyrimidine derivatives. Journal of Heterocyclic Chemistry, 43(5), 1327–1329. https://doi.org/10.1002/jhet.5570430527

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