HRID602448

反应详情

EQUATION

反应方程式

HRID 602448 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a stirred suspension of lithium aluminum hydride (97 mg, 2.55 mmol) in tetrahydrofuran (5 mL) was added a solution of ethyl [cis-5-amino-1-benzylpiperidin-2-yl]acetate (352 mg, 1.27 mmol, step 7 of Example 1) in tetrahydrofuran (4 mL) at 0° C., and the mixture was stirred at 0° C. for 1 h, then stirred at room temperature for 1 h. The mixture was quenched with water (0.1 mL) at 0° C., and stirred for 30 min at 0° C. 15% aqueous sodium hydroxide solution (0.1 mL) was added at 0° C., and the mixture was stirred at room temperature for 30 min. Water (0.3 mL) was added, and the mixture was stirred at room temperature for 30 min. The mixture was filtered through Celte pad washing with tetrahydrofuran (100 mL). The filtrate was concentrated under reduced pressure to give 322 mg (quant.) of the title compound as a slightly yellow oil.

WORKUP

后处理

  1. stirringstirred at room temperature for 1 h
  2. customThe mixture was quenched with water (0.1 mL) at 0° C.
  3. stirringstirred for 30 min at 0° C
  4. addition15% aqueous sodium hydroxide solution (0.1 mL) was added at 0° C.
  5. stirringthe mixture was stirred at room temperature for 30 min
  6. additionWater (0.3 mL) was added
  7. stirringthe mixture was stirred at room temperature for 30 min
  8. filtrationThe mixture was filtered through Celte pad
  9. washwashing with tetrahydrofuran (100 mL)
  10. concentrationThe filtrate was concentrated under reduced pressure