HRID1279213

反应详情

EQUATION

反应方程式

HRID 1279213 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

2-Chloroethanesulfonyl chloride (0.12 ml, 1.16 mmol) was added to a solution of (2S,3S,4R,5R)-5-{2-(aminomethyl)-6-[(2,2-diphenylethyl)amino]-9H-purin-9-yl}-N-ethyl-3,4-dihydroxytetrahydro-2-furancarboxamide (Preparation 27) (600 mg, 1.16 mmol) in a mixture of pyridine (2.5 ml ) and acetonitrile (10 ml). The reaction mixture was stirred for 1 hour at room temperature. Piperidine (1.0 ml, 10 mmol) was then added and the reaction mixture was heated under reflux for 16 hours. The reaction mixture was then diluted with ethyl acetate (50 ml) and washed with water (30 ml). The ethyl acetate layer was dried (anhydrous magnesium sulphate) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol:ammonia (95:5:0.5 by volume) increasing in polarity to dichloromethane:methanol:ammonia (90:10:1 by volume). The solvent was removed under reduced pressure and the residue repurified by column chromatography on silica gel eluting with ethyl acetate:methanol:ammonia (95:5:0.5 by volume) increasing in polarity to ethyl acetate:methanol:ammonia (90:10:1 by volume). The solvent was removed under reduced pressure and the residue was repurified by column chromatography on silica gel eluting with ethyl acetate:methanol (95:5 by volume) increasing in polarity to ethyl acetate:methanol (90:10 by volume) then ethyl acetate:methanol:ammonia (90:10:1 by volume). The solvent was removed under reduced pressure to give the title compound (21 mg).

WORKUP

后处理

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 16 hours
  3. washwashed with water (30 ml)
  4. dry with materialThe ethyl acetate layer was dried (anhydrous magnesium sulphate)
  5. customevaporated under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol:ammonia (95:5:0.5 by volume)
  7. temperatureincreasing in polarity to dichloromethane:methanol:ammonia (90:10:1 by volume)
  8. customThe solvent was removed under reduced pressure
  9. customthe residue repurified by column chromatography on silica gel eluting with ethyl acetate:methanol:ammonia (95:5:0.5 by volume)
  10. temperatureincreasing in polarity to ethyl acetate:methanol:ammonia (90:10:1 by volume)
  11. customThe solvent was removed under reduced pressure
  12. customthe residue was repurified by column chromatography on silica gel eluting with ethyl acetate:methanol (95:5 by volume)
  13. temperatureincreasing in polarity to ethyl acetate:methanol (90:10 by volume)
  14. customThe solvent was removed under reduced pressure