Nguyen-Ba N, Lee N, Chan L, Zacharie B
BioChem Pharma Inc., Laval, Quebec, Canada.
Bioorg Med Chem Lett. 2000 Oct 2;10(19):2223-6. doi: 10.1016/s0960-894x(00)00452-2.
Two series of 1,3-dioxolanes and 1,3-oxathiolane nucleosides containing N-9-oxypurine were synthesized as potential antiviral agents. These compounds were prepared by reacting the sugar moieties with iodo- or bromotrimethylsilane, followed by treatment with a mixture of sodium hydride and the desired N-hydroxy purine base. The preparation of these N-hydroxybases was also described. No significant antiviral activity was observed against HIV, HBV, HSV-1, HSV-2, or HCMV.
合成了两个系列含N-9-氧代嘌呤的1,3-二氧戊环和1,3-氧硫杂环戊烷核苷作为潜在的抗病毒剂。这些化合物是通过使糖部分与碘代或溴代三甲基硅烷反应,然后用氢化钠和所需的N-羟基嘌呤碱的混合物处理来制备的。还描述了这些N-羟基碱的制备方法。未观察到对HIV、HBV、HSV-1、HSV-2或HCMV有显著的抗病毒活性。