HRID1251879

反应详情

EQUATION

反应方程式

HRID 1251879 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of N-(2-hydroxy-2-methylpropyl)morpholine (9.8 g, 62 mmol), N-benzyloxycarbonyl-L-methionine (12.6 g, 44 mmol), bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (25 g, 54 mmol), DMAP (5.4 g, 44 mmole) in dichloromethane (250 ml) was stirred, in the presence of 4 Å molecular sieves (5 g), at ambient temperature for 48 h. After evaporation to dryness, the mixture was taken up in diethyl ether and the insoluble material eliminated by filtration. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and a saturated solution of brine, evaporated to dryness and purified by flash column chromatography eluting with dichloromethane/ethanol (98:2) to give 2-(morpholinomethyl)prop-2-yl (2S)-2-(benzyloxycarbonylamino)-4-methylsulfanylbutyrate (40%).

WORKUP

后处理

  1. customAfter evaporation to dryness
  2. filtrationthe insoluble material eliminated by filtration
  3. washThe organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate
  4. customa saturated solution of brine, evaporated to dryness
  5. custompurified by flash column chromatography
  6. washeluting with dichloromethane/ethanol (98:2)