Synthesis of 2,4,6-trisubstituted pyrimidines as antimalarial agents

A series of 2,4,6-trisubstituted-pyrimidines were synthesized and evaluated for their in vitro antimalarial activity against Plasmodium falciparum. Of the 18 compounds synthesized, 14 compounds have shown MIC in the range of 0.25–2 μg/mL. These compounds are in vitro severalfold more active than pyrimethamine.

A series of 2,4,6-trisubstituted-pyrimidines were synthesized and evaluated for their in vitro antimalarial activity. Of the 18 compounds synthesized, 14 compounds showed MIC in the range of 0.25–2 μg/mL.Figure optionsDownload as PowerPoint slide