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Formation of 4-aminopyrimidines via the trimerization of nitriles using focused microwave heating.

Journal of combinatorial chemistry (2005-05-10)
Ian R Baxendale, Steven V Ley
RESUMO

A series of substituted aliphatic nitriles have been trimerized to their corresponding pyrimidine structures under solvent-free conditions in the presence of catalytic quantities of potassium tert-butoxide using a focused microwave reactor. Multigram quantities of the corresponding 4-aminopyrimidines have been prepared in high yields and purity following a simple and scaleable protocol.

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Sigma-Aldrich
Potassium tert-butoxide, reagent grade, ≥98%
Sigma-Aldrich
Terc-butóxido de potássio, 1.0 M in THF
Sigma-Aldrich
Potassium tert-butoxide, sublimed grade, 99.99% trace metals basis
Sigma-Aldrich
4-Aminopyrimidine, 98%