HRID1617

反应详情

EQUATION

反应方程式

HRID 1617 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

N-Carboxy-[1-butylpiperidin-4-ylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazole (0.530 g, 1.32 mmol) was dissolved in chloroform (25 ml) and treated with 2,3-dichloro-5,6-dicyano-1, 4-benzoquinone (0.329 g, 1.58 mmol) with stirring. The mixture was heated to reflux for 12 hours, cooled, and more 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.329 g 1.58 mmol) added with stirring. The mixture was heated to reflux for 12 hours, cooled and evaporated under reduced pressure. The residue was purified by Silica-gel chromatography, eluting with 2%MeOH/CHCl3 to give the title compounds as 3:1 mixture. The mixture was separated by preparative HPLC using a Waters Micro Bondapak C18 (300 mm×7.8 mm) column and eluting with 75:25 MeCN: 0.1M Ammonium Acetate (pH 5.0).

WORKUP

后处理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 12 hours
  3. temperaturecooled
  4. stirringwith stirring
  5. temperatureThe mixture was heated
  6. temperatureto reflux for 12 hours
  7. temperaturecooled
  8. customevaporated under reduced pressure
  9. customThe residue was purified by Silica-gel chromatography
  10. washeluting with 2%MeOH/CHCl3