HRID1518252

反应详情

EQUATION

反应方程式

HRID 1518252 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

DMSO (5 eq.) was dissolved in DCM and the solution was cooled to −78° C. To the stirred solution oxalylchloride (2.5 eq.) was added and the mixture was left stirring for 30 min. A solution of methyl 1-allyl-3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1H-indole-6-carboxylate (1 eq.) in DCM (0.25M solution) was added and the mixture was left stirring for 30 min at −78° C. Et3N (8 eq.) was added and the mixture was allowed to warm to 0° C. At this temperature stirring was continued for 2 h, and then stirring was continued at RT overnight. The mixture was diluted with DCM, and then washed with water, 1N HCl, saturated aq. NaHCO3 solution and with brine. After drying over Na2SO4 all volatiles were evaporated in vacuo. The residual material was purified by flash chromatography (PE:EtOAc, 9:1). After evaporation of the solvents the product was obtained as a yellow foam (88%). MS (ES+): 432.1 (M+H+).

WORKUP

后处理

  1. waitthe mixture was left
  2. waitthe mixture was left
  3. stirringstirring for 30 min at −78° C
  4. temperatureto warm to 0° C
  5. stirringAt this temperature stirring
  6. waitwas continued for 2 h
  7. stirringstirring
  8. waitwas continued at RT overnight
  9. washwashed with water, 1N HCl, saturated aq. NaHCO3 solution and with brine
  10. dry with materialAfter drying over Na2SO4 all volatiles
  11. customwere evaporated in vacuo
  12. customThe residual material was purified by flash chromatography (PE:EtOAc, 9:1)
  13. customAfter evaporation of the solvents the product