HRID986987

反应详情

EQUATION

反应方程式

HRID 986987 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

To a solution of 3-benzyl4-oxo-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (1935.97 g, 5.36 mol) in toluene (9700 mL) was added methylhydrazine (299.2 mL, 5.63 mol), followed by acetic acid (325 mL, 5.68 mol) slowly at about 8° C. The reaction mixture was heated slowly to about 65° C. and stirred for about 7.5 hours. After cooling to room temperature, the organic layer was washed with 10% sodium bicarbonate, water and saturated NaCl solution and concentrated in vacuo to a low volume. The reaction was repeated at same scale twice. The concentrated product solutions from the three reactions were combined and mixed with IPE (50 L), cooled to about 0° C., HCl gas was introduced repeatedly and stirred at room temperature overnight until the deprotection was complete. The mixture was concentrated in vacuo to about half of the original volume, methylene chloride (24 L) was added, followed by NH4OH (22 L). The mixture was then extracted with methylene chloride and concentrated to a low volume (6 to 7 L). Hexane (20 L) was added and the mixture was cooled to about 15-20° C. The free base product was collected as crystals and dried under vacuum (2985 g total, yield 84.8%).

WORKUP

后处理

  1. temperatureAfter cooling to room temperature
  2. washthe organic layer was washed with 10% sodium bicarbonate, water and saturated NaCl solution
  3. concentrationconcentrated in vacuo to a low volume
  4. additionmixed with IPE (50 L)
  5. temperaturecooled to about 0° C.
  6. additionHCl gas was introduced repeatedly
  7. stirringstirred at room temperature overnight until the deprotection
  8. concentrationThe mixture was concentrated in vacuo to about half of the original volume, methylene chloride (24 L)
  9. additionwas added
  10. extractionThe mixture was then extracted with methylene chloride
  11. concentrationconcentrated to a low volume (6 to 7 L)
  12. additionHexane (20 L) was added
  13. temperaturethe mixture was cooled to about 15-20° C
  14. customThe free base product was collected as crystals
  15. customdried under vacuum (2985 g total, yield 84.8%)