Synthesis of new uracil non-nucleoside derivatives as potential inhibitors of HIV-1
作者:Farag A. El-Essawy、Nasser R. El-Brollosy、Erik B. Pedersen、Claus Nielsen
DOI:10.1002/jhet.5570400203
日期:2003.3
6-(2-Phenylethyl) and 6-cyclohexyl 5-cyanouracils (1a,b) were synthesized and reacted with chloromethyl ethyl ether, benzyl chloromethyl ether, chloromethyl methyl sulfide and (2-acetoxyethoxy)methyl bromide. New uracil analogues of (S)-DHPA were synthesized by reaction of compounds (1a,b) with ((S)-2,2-dimethyl-1,3-dioxolane-4-yl) alkyl p-toluenesulfonate.
合成6-(2-苯基乙基)和6-环己基5-氰尿嘧啶(1a,b),并使其与氯甲基乙基醚,苄基氯甲基甲基醚,氯甲基甲基硫醚和(2-乙酰氧基乙氧基)甲基溴反应。通过化合物(1a,b)与对甲苯磺酸((S)-2,2-二甲基-1,3-二氧戊环-4-基)烷基酯的反应合成了(S)-DHPA的新尿嘧啶类似物。