HRID128947

反应详情

EQUATION

反应方程式

HRID 128947 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A solution of the alcohol prepared in Step (a) (1.98 g, 0.01 mol), N,N-diisopropylethylamine (3.5 mL, 0.02 mol) and a catalytic amount of 4-dimethylaminopyridine is cooled to 0° C., and methanesulfonyl chloride (0.8 mL, 0.0105 mol) is added dropwise. The solution is stirred at 0° C. for 18 hours, and then concentrated under reduced pressure. The residue is taken up in dimethylformamide (20 mL), and to this solution is added 4-phenyl-1,2,3,6-tetrahydropyridine (2.41 g, 0.015 mol) and sodium bicarbonate (3.4 g, 0.04 mol). The mixture is heated at 40° C. for 5 hours, and the solvent is removed under reduced pressure. The residue is partitioned between 50 mL of ethyl acetate and 50 mL of water. The aqueous layer is extracted with 50 mL of ethyl acetate and the combined organic layers are dried (sodium sulfate), and the solvent is removed in vacuo. The residue is chromatographed (silica gel, 2% methanol/ 98% dichloromethane) to give the title compound, containing 0.4 mol of water; mp 94.3°-95.8° C.

WORKUP

后处理

  1. concentrationconcentrated under reduced pressure
  2. temperatureThe mixture is heated at 40° C. for 5 hours
  3. customthe solvent is removed under reduced pressure
  4. customThe residue is partitioned between 50 mL of ethyl acetate and 50 mL of water
  5. extractionThe aqueous layer is extracted with 50 mL of ethyl acetate
  6. dry with materialthe combined organic layers are dried (sodium sulfate)
  7. customthe solvent is removed in vacuo
  8. customThe residue is chromatographed (silica gel, 2% methanol/ 98% dichloromethane)