反应 #1880979

ord-80103e80c64444f89518837dd029ac88

反应方程式

O[C@@H]1[C@H](O)[C@@H](C=Cc2ccc(F)cc2)O[C@H]1n1cnc2c(NC3CCOC3)ncnc21
5-[2-(4-fluorophenyl)vinyl](4S,2R,3R,5R)-2-[6-(oxolan-3-ylamino)purin-9-yl]oxolane-3,4-diol
O[C@@H]1[C@H](O)[C@@H](CCc2ccc(F)cc2)O[C@H]1n1cnc2c(NC3CCOC3)ncnc21
(4S,2R,3R,5R)-5-[2-(4-fluorophenyl)ethyl]-2-[6-(oxolan-3-ylamino)purin-9-yl]oxolane-3,4-diol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The catalyst was filtered off
  2. 2
    其他solvent removed under reduced pressure
  3. 3
    其他The residue was purified by preparative thin layer chromatography

实验过程

To a solution of 5-[2-(4-fluorophenyl)vinyl](4S,2R,3R,5R)-2-[6-(oxolan-3-ylamino)purin-9-yl]oxolane-3,4-diol (40 mg) in ethanol (5 ml) and cyclohexene (2 ml) was added palladium hydroxide (50 mg), and the mixture was stirred for 24 hours. The catalyst was filtered off, and solvent removed under reduced pressure. The residue was purified by preparative thin layer chromatography, to give pure (4S,2R,3R,5R)-5-[2-(4-fluorophenyl)ethyl]-2-[6-(oxolan-3-ylamino)purin-9-yl]oxolane-3,4-diol, a compound of Formula I.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07022681B2uspto-grants-2006_04