HRID1291553

反应详情

EQUATION

反应方程式

HRID 1291553 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

In 10 ml of dimethylformamide were dispersed 0.4 g of 5-[2-(p-toluenesulfonyloxy)ethoxy]-7-fluoro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine, 0.38 ml of N-methylpiperazine and 0.3 g of sodium iodide. The dispersion was stirred at room temperature for 3 days. The reaction mixture was concentrated. The residue was mixed with water and the mixture was subjected to extraction with ethyl acetate. The extract was dried over sodium carbonate and purified by silica gel column chromatography (elutant: dichloromethane/-methanol=10/1) to obtain 1.15 g of 5-[2-(4-methyl-1-piperazinyl)ethoxy]-7-fluoro-1-[2-methoxy-4-(2-methyl-benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine. Colorless and amorphous

WORKUP

后处理

  1. concentrationThe reaction mixture was concentrated
  2. additionThe residue was mixed with water
  3. extractionthe mixture was subjected to extraction with ethyl acetate
  4. dry with materialThe extract was dried over sodium carbonate
  5. custompurified by silica gel column chromatography (elutant: dichloromethane/-methanol=10/1)