HRID1424192

反应详情

EQUATION

反应方程式

HRID 1424192 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

N-Boc-L-allo-threonine (Preparation 54, 67.12 g, 306 mmol), 4-tert-butyl-diaminobenzene (60.3 g, 367 mmol) and HOBt (56.3 g, 367 mmol) were dissolved in DMF (500 mL). NMM (67 mL, 612 mmol) was added and the mixture cooled to 0° C. EDCI (65.6 g, 336 mmol) was added portionwise over 1.5 hours and the reaction was stirred at room temperature for 18 hours. EtOAc (2 L) was added followed by water (10 and the mixture stirred vigorously for 15 minutes. The aqueous layer was removed and washed further with EtOAc (2×30 mL). The organic layers were combined, dried over Na2SO4 and concentrated in vacuo. The residue was sonicated in pentane/DCM 10/1 twice and filtered to afford a pale pink solid that was dissolved in AcOH (500 mL) and stirred at 40° C. for 24 hours followed by room temperature for 2 days. The solvent was removed in vacuo and the residue dissolved in EtOAc (1.5 L). Saturated aqueous NaHCO3 (500 mL) was added and the mixture stirred vigorously. The organic layer was collected, washed with NaHCO3 solution (2×200 mL), dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in DCM (500 mL) and purified using silica gel column chromatography eluting with 0-20% acetone in cyclohexaneto afford the title compound as an off-white solid (89 g, quant).

WORKUP

后处理

  1. stirringthe mixture stirred vigorously for 15 minutes
  2. customThe aqueous layer was removed
  3. washwashed further with EtOAc (2×30 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was sonicated in pentane/DCM 10/1 twice
  7. filtrationfiltered
  8. customto afford a pale pink solid
  9. stirringstirred at 40° C. for 24 hours
  10. waitfollowed by room temperature for 2 days
  11. customThe solvent was removed in vacuo
  12. dissolutionthe residue dissolved in EtOAc (1.5 L)
  13. additionSaturated aqueous NaHCO3 (500 mL) was added
  14. stirringthe mixture stirred vigorously
  15. customThe organic layer was collected
  16. washwashed with NaHCO3 solution (2×200 mL)
  17. dry with materialdried over Na2SO4
  18. concentrationconcentrated in vacuo
  19. dissolutionThe residue was dissolved in DCM (500 mL)
  20. custompurified
  21. washeluting with 0-20% acetone in cyclohexaneto