申请人:Bristol-Myers Squibb Company
公开号:EP0428109A2
公开(公告)日:1991-05-22
There is disclosed a process for synthesizing 2′-fluoro-2′,3′-dideoxyarabinofuranose derivatives of inosine and adenine on a large scale which involves coupling of a fluorosugar derivative and a purine reactant to provide a purine nucleoside intermediate which is then deoxygenated. 6-Chloro or 6-benzamidopurine and 1,3,5-tri-O-benzoyl-2-deoxy-2-fluoroarabinofuranose are used as starting materials.
本发明公开了一种大规模合成肌苷和腺嘌呤的 2′-氟-2′,3′-二脱氧阿拉伯呋喃糖衍生物的工艺,该工艺包括将一种氟糖衍生物和一种嘌呤反应物偶联,以提供一种嘌呤核苷中间体,然后将其脱氧。6-Cloro 或 6-benzamidopurine 和 1,3,5-tri-O-benzoyl-2-de-deoxy-2-fluoroarabinofuranose 可用作起始原料。