HRID619805

反应详情

EQUATION

反应方程式

HRID 619805 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of Boc-L-serine (10.3 g, 50 mmol) in 75 mL of H2O:t-BuOH (2:1) is added methoxyamine hydrochloride (23 g, 75 mmol) and 1-(3-dimethyl-aminopropyl)-3-ethylcarbodiimide hydrochloride (9.6 g, 50 mmol). After 2 hours, the solution is saturated with NaCl. The solution is extracted with EtOAc. The organic layer is dried over MgSO4, filtered and concentrated. The resulting crude material is dissolved in 50 mL of pyridine and cooled to 0° C. To the solution is added methane sulfonyl chloride (7.44 g, 65 mmol). After 1 hour, the solution is poured into 100 mL of cold 1 N HCl (aq.). The solution is diluted with EtOAc. The layers are separated and the organic layer is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The resulting crude material is dissolved in 50 mL of acetone and added dropwise to a solution of K2CO3 (20.7 g, 150 mmol) in 900 mL of acetone at reflux. After 1 hour, the solution is cooled to ambient temperatures. The solution is filtered through Celite. The collected organic solution is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The resulting solid is dissolved in 20 mL of THF and added dropwise to an ammonia solution containing sodium (2.6 g, 113 mmol) at -78° C. After the blue color has dissipated, the solution is stirred for an additional 10 minutes. To the reaction mixture is added NH4Cl (13.4 g, 250 mmol) and the solution is allowed to warm to ambient temperatures. The solution is filtered. The collected solution is concentrated. The resulting residue is recrystallized from EtOAc to give the title compound (2 g, 11 mmol) as a white solid.

WORKUP

后处理

  1. extractionThe solution is extracted with EtOAc
  2. dry with materialThe organic layer is dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. dissolutionThe resulting crude material is dissolved in 50 mL of pyridine
  6. waitAfter 1 hour
  7. customThe layers are separated
  8. washthe organic layer is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl
  9. dry with materialThe organic layer is dried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated
  12. dissolutionThe resulting crude material is dissolved in 50 mL of acetone
  13. temperatureat reflux
  14. waitAfter 1 hour
  15. temperaturethe solution is cooled to ambient temperatures
  16. filtrationThe solution is filtered through Celite
  17. washThe collected organic solution is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl
  18. dry with materialThe organic layer is dried over MgSO4
  19. filtrationfiltered
  20. concentrationconcentrated
  21. dissolutionThe resulting solid is dissolved in 20 mL of THF
  22. additionadded dropwise to an ammonia solution
  23. temperatureto warm to ambient temperatures
  24. filtrationThe solution is filtered
  25. concentrationThe collected solution is concentrated
  26. customThe resulting residue is recrystallized from EtOAc