Synthesis and in vitro anti-HIV activity of certain 2-(1H-benzimidazol-2-ylamino)pyrimidin-4(3H)-ones and related derivatives

Article abstract of DOI:10.1002/ardp.19973300304

In an ongoing effort to develop novel non-nucleoside human immunodeficiency virus inhibitors, a series of substituted 2-(1H)-benzimidazol-2-ylamino)pyrimidin-4-(3H)-ones and related derivatives were synthesized via cyclocondensation of 2-guanidono-1H-benzimidazole with diethyl ethoxymethylenemalonate, substituted diethyl malonates, some β-keto esters and 2-acetylbutyrolactone. From these series of compounds, 2-(1H-benzimidazol-2-ylamino)-6-hydroxy-5-phenylpyrimidin-4(3H)-ones (5f, NSC 66628) was confirmed to have a moderate in vitro anti-HIV activity.