扎西他滨前药的合成与结构表征

Synthesis and characterization of Zalcitabine prodrugs

以抗艾滋病药物扎西他滨为先导物与取代桂皮酸缩合,合成了4个O-取代桂皮酰基-N-取代桂皮酰基-2’,3’-双脱氧胞苷衍生物,并用IR,1H NMR和MS方法对新化合物的结构进行了确证.

By using anti AIDS agents Zalcitabine as lead compound,from which four N-substituted cinnamyl-O-substituted cinnamyl-2＇,3＇-Dideoxycytidine derivatives were synthesized via condensation with the corresponding substituted cinnamic acids.The chemical structures of the new compounds were characterized by IR,1H NMR and MS.