HRID1988593

反应详情

EQUATION

反应方程式

HRID 1988593 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 2-chloro-4-methylamino-pyrimidine-5-carbaldehyde (1.08 g, 6.3 mmol) and N-(3-amino-4-methyl-phenyl)-3-trifluoromethylbenzamide (2.04 g, 6.9 mmol) in MeOH (70 mL) is stirred for 2 hours at 45° C. and then treated with sodium cyanoborohydride (1.19 g, 18.9 mmol) and acetic acid (1 mL) sequentially. After stirring for 2 hours at room temperature, the reaction mixture is diluted with CHCl3 and washed with saturated NaHCO3. The organic layer is dried over MgSO4 and concentrated under reduced pressure. The residue is purified by flash column chromatography (SiO2, EtOAc/hexane=1/2) to give N-{3-[(2-chloro-4-methylaminopyrimidin-5-ylmethyl)amino]-4-methylphenyl}-3-trifluoromethylbenzamide (1.80 g, 64%) as a white solid.

WORKUP

后处理

  1. washwashed with saturated NaHCO3
  2. dry with materialThe organic layer is dried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. customThe residue is purified by flash column chromatography (SiO2, EtOAc/hexane=1/2)