HRID4025

反应详情

EQUATION

反应方程式

HRID 4025 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of N-[2-(5-bromo-1-indolinyl)phenyl]phenylcarbamate (11.5 g, 28.5 mmoles), N-methylpiperazine (15 ml) and ether (50 ml) was stirred at room temperature for 2 hours. The ether was evaporated. The mixture was filtered through a silica gel column (150 g), packed with dichloromethaane, and the column was washed with 2% methanol-dichloromethane solution (2 l). The solvent was evaporated. The residue was purified by flash chromatography on a silica gel column (150 g, 230-400 mesh), eluted with 1% methanol/dichloromethane (4 l), 1.5% methanol/dichloromethane (2 l), and 2% methanol/dichloromethane. The fractions containing the desired material were collected and evaporated to give 10.9 g (90%) of product. Crystallization from chloroform and hexane afforded the analytical sample, mp 108°-110° C.

WORKUP

后处理

  1. customThe ether was evaporated
  2. filtrationThe mixture was filtered through a silica gel column (150 g)
  3. washthe column was washed with 2% methanol-dichloromethane solution (2 l)
  4. customThe solvent was evaporated
  5. customThe residue was purified by flash chromatography on a silica gel column (150 g, 230-400 mesh)
  6. washeluted with 1% methanol/dichloromethane (4 l), 1.5% methanol/dichloromethane (2 l), and 2% methanol/dichloromethane
  7. additionThe fractions containing the desired material
  8. customwere collected
  9. customevaporated