Formation of 4-aminopyrimidines via the trimerization of nitriles using focused microwave heating.
Ian R Baxendale, Steven V Ley
Index: J. Comb. Chem. 7(3) , 483-9, (2005)
Full Text: HTML
Abstract
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.
Related Compounds
Related Articles:
Silylation of C-H bonds in aromatic heterocycles by an Earth-abundant metal catalyst.
2015-02-05
[Nature 518(7537) , 80-4, (2015)]
2015-06-05
[Carbohydr. Polym. 123 , 432-42, (2015)]
2003-02-05
[J. Pharm. Biomed. Anal. 31(1) , 63-74, (2003)]
2015-09-01
[Acta Biomater. 23 , 250-62, (2015)]
2015-10-26
[Chemistry 21 , 15759-68, (2015)]