HRID2188026

反应详情

EQUATION

反应方程式

HRID 2188026 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

4,4-Diethoxy-1-((S)-1-phenyl-ethyl)-(R)-2-aminomethyl-piperidine (2.25 g, 7.37 mmol), and triethyl amine (1.49 g, 14.7 mmol) in acetonitrile (50 ml) was heated to 60° C. before 2-chlormethyl-6-methoxy-benzoic acid methyl ester (1.58 g, 7.37 mmol) in acetonitrile (25 ml) was added over the course of 1.5 hour. After addition the reaction mixture was stirred overnight at 60° C. The solvent was removed in vacuo and the residue was dissolved in dichloromethane (50 ml) and washed with saturated sodium bicarbonate. After drying (MgSO4), filtration and evaporation of the solvent in vacuo the residue was subjected to flash column chromatography (SiO2, ethyl acetate-light petrol ether (1:1)) to give 2.3 g (69%) of 2-(R)-(7-methoxy-2,3-dihydro-isoindol-1-one-2-ylmethyl)-4,4-diethoxy-1-(1-(S)-phenyl-ethyl)-piperidine.

WORKUP

后处理

  1. additionwas added over the course of 1.5 hour
  2. additionAfter addition the reaction mixture
  3. customThe solvent was removed in vacuo
  4. dissolutionthe residue was dissolved in dichloromethane (50 ml)
  5. washwashed with saturated sodium bicarbonate
  6. customAfter drying
  7. filtration(MgSO4), filtration and evaporation of the solvent in vacuo the residue