HRID2265863

反应详情

EQUATION

反应方程式

HRID 2265863 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a stirred solution of 3-methyl-6-aminoindazole (2.71 g, 0.015 mol) and NaHCO3 (1.26 g, 0.045 mol) in THF (15 mL) and ethanol (60 mL) was added 2,4-dichloropyrimidine (6.66 g, 0.045 mol) at room temperature. After the reaction was stirred for four hours, the suspension was filtered and washed thoroughly with ethanol. The filtrate was concentrated under reduced pressure, and the resulting solid was washed with ether to remove excess pyrimidine to yield 3.5 g (89% yield) of N-(2-chloro-4-pyrimidinyl)-N-(3-methyl-1H-indazol-6-yl)amine.

WORKUP

后处理

  1. filtrationthe suspension was filtered
  2. washwashed thoroughly with ethanol
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. washthe resulting solid was washed with ether
  5. customto remove excess pyrimidine