HRID217282

反应详情

EQUATION

反应方程式

HRID 217282 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Triethylamine (12 μL) and 2-methoxybenzenethiol (12 mg) were added in succession to a solution of the above-described [5-(4-amino-6-phenylmethanesulfinyl-[1,3,5]triazin-2-yl)-2,4-dichlorophenoxy]-acetonitrile (12 mg) in dimethylformamide (0.5 mL). The mixture was stirred at room temperature for 8 hours. After dilution with ethyl acetate (7 mL), the mixture was washed twice with water and once with brine. The mixture was pre-dried over anhydrous sodium sulfate, and filtered. The solvent was distilled off. The resulting residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3) to give {5-[4-amino-6-(2-methoxy-phenylsulfanyl)-[1,3,5]triazin-2-yl]-2,4-dichlorophenoxy}-acetonitrile as white solid (10 mg).

WORKUP

后处理

  1. washAfter dilution with ethyl acetate (7 mL), the mixture was washed twice with water and once with brine
  2. dry with materialThe mixture was pre-dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. distillationThe solvent was distilled off
  5. customThe resulting residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3)