HRID1066181

反应详情

EQUATION

反应方程式

HRID 1066181 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

Ethyl 4-{3-[4-amino-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoate (22.8 g) was dissolved in N,N-dimethylformamide (115 ml), and 1-(2-methoxyphenyl)piperazine hydrochloride (12.9 g), potassium iodide (17.1 g), potassium carbonate (17.8 g) were added to the solution. The thus-produced mixture was stirred at 90° C. for one hour. The reaction mixture was cooled and diluted with ethyl acetate (200 ml). The formed solution was sequentially washed with water and saturated brine, and dried. The solution was concentrated under reduced pressure. A′4N solution (28 ml) of hydrochloric acid in dioxane was added to the residue, and crystals so precipitated were collected by filtration. The collected crystals were recrystallized from ethanol, to thereby obtain 27.4 g of ethyl 4-{3-{4-amino-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoate hydrochloride as yellow crystals.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled
  2. washThe formed solution was sequentially washed with water and saturated brine
  3. customdried
  4. concentrationThe solution was concentrated under reduced pressure
  5. additionA′4N solution (28 ml) of hydrochloric acid in dioxane was added to the residue, and crystals
  6. customso precipitated
  7. filtrationwere collected by filtration
  8. customThe collected crystals were recrystallized from ethanol