HRID381338

反应详情

EQUATION

反应方程式

HRID 381338 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 3-{1-(1,3-benzodioxol-5-yl)-2-[(2-methoxy-4-methylphenyl)sulfonamido]-2-oxoethyl}-6-bromo-1-methyl-1H-indole (from Example 85, 300 mg, 0.53 mmol), ethyl vinyl ether (0.063 ml), palladium(II)acetate (6 mg), tri-o-tolylphosphine (13 mg) and triethylamine (0.1 ml) in acetonitrile (5 ml) was heated at reflux for 18 hours under a nitrogen atmosphere. After cooling, the solvent was evaporated in vacuo and the residue was stirred with 2N hydrochloric acid (˜6 ml) for 45 minutes. The mixture was twice extracted with ethyl acetate, and then washed with water, and brine, The organic layer was dried (magnesium sulphate) and the solvents were evaporated in vacuo. The residue was flash chromatographed using a gradient elution of a mixture of 90% hexane and 10% ethyl acetate, through to 40% hexane and 60% ethyl acetate, to give the title compound (80 mg).

WORKUP

后处理

  1. temperaturewas heated
  2. temperatureat reflux for 18 hours under a nitrogen atmosphere
  3. temperatureAfter cooling
  4. customthe solvent was evaporated in vacuo
  5. extractionThe mixture was twice extracted with ethyl acetate
  6. washwashed with water, and brine
  7. dry with materialThe organic layer was dried (magnesium sulphate)
  8. customthe solvents were evaporated in vacuo
  9. customchromatographed
  10. washa gradient elution of a mixture of 90% hexane and 10% ethyl acetate