HRID562544

反应详情

EQUATION

反应方程式

HRID 562544 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

4-[(15-tert-butoxycarbonylpentadecanoylamino)methyl]benzoic acid (413 mg, 0.868 mmol) was dissolved in THF (5 mL), the solution was cooled with an icebath. DIPEA (0.33 mL, 1.91 mmol) and TSTU (314 mg, 1.04 mmol) were added. The mixture was stirred under nitrogen while cooling was maintained. After 30 minutes the icebath was removed and the mixture was stirred for additional 3 hours at room temperature. The mixture was diluted with NMP (5 mL) and H-GluOtBu (0.21 g, 1.04 mmol) was added, the mixture was stirred overnight at room temperature. The mixture was separated between ethyl acetate (100 mL) and water (100 mL), the organic phase dried (Na2SO4) and solvent removed in vacuo. The crude material was purified on silica using DCM/ethanol (90:10) to give (S)-2-{4-[(15-tert-Butoxycarbonyl-pentadecanoylamino)-methyl]-benzoylamino}-pentanedioic acid 1-tert-butyl ester.

WORKUP

后处理

  1. temperaturethe solution was cooled with an icebath
  2. temperaturewhile cooling
  3. temperaturewas maintained
  4. customAfter 30 minutes the icebath was removed
  5. stirringthe mixture was stirred for additional 3 hours at room temperature
  6. additionwas added
  7. stirringthe mixture was stirred overnight at room temperature
  8. customThe mixture was separated between ethyl acetate (100 mL) and water (100 mL)
  9. dry with materialthe organic phase dried (Na2SO4) and solvent
  10. customremoved in vacuo
  11. customThe crude material was purified on silica