HRID642288

反应详情

EQUATION

反应方程式

HRID 642288 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

A mixture of 4-[(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester (302 mg, 0.58 mol) in THF (5 mL) was added drop wise a solution of 1 M KOtBu in THF (702 μL, 0.70 mmol) at −78° C. The mixture was stirred at −78° C. for 15 min, warmed to room temperature and stirred at that temperature for 1.5 h before it was quenched with brine, extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to a yellow foam (469 mg). It was dissolved in dichloromethane (10 mL) and TFA (2.5 mL) was added. The mixture was stirred at room temperature for 1 h before it was concentrated in vacuo. It was redissolved in dichloromethane, triethylamine (923 μL) was added. The mixture was stirred under air overnight before it was partitioned between dichloromethane and water, the organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and dichloromethane to give the title compound as a white solid (257 mg): MS: (+) m/z 330.0 (M+1).

WORKUP

后处理

  1. temperaturewarmed to room temperature
  2. stirringstirred at that temperature for 1.5 h before it
  3. customwas quenched with brine
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated in vacuo to a yellow foam (469 mg)
  8. dissolutionIt was dissolved in dichloromethane (10 mL)
  9. additionTFA (2.5 mL) was added
  10. stirringThe mixture was stirred at room temperature for 1 h before it
  11. concentrationwas concentrated in vacuo
  12. dissolutionIt was redissolved in dichloromethane
  13. additiontriethylamine (923 μL) was added
  14. stirringThe mixture was stirred under air overnight before it
  15. customwas partitioned between dichloromethane and water
  16. washthe organic layer was washed with brine
  17. dry with materialdried over anhydrous sodium sulfate
  18. concentrationconcentrated in vacuo
  19. customThe residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and dichloromethane