HRID1530649

反应详情

EQUATION

反应方程式

HRID 1530649 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

To a solution of tert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylate (500 mg, 2.20 mmol) in THF (50 mL) was added DIBAl-H (22 mL, 22 mmol) under nitrogen atmosphere. The resulting mixture was stirred at 25° C. overnight. Methanol (5 mL) was added to quench the reaction at −78° C. After being stirred at room temperature for 1 h, water (10 mL) was added. The solid was filtered off and washed with EtOAc. The combined filtrate was partitioned and extracted with EtOAc (3×50 mL), dried over Na2SO4, and concentrated. The residue was purified by silica gel chromatography eluting with EtOAc/petroleum ether (1:10) to give tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate (350 mg, 69% yield) as a colorless oil. LCMS (ESI) m/z: 230.4 [M+H+].

WORKUP

后处理

  1. customto quench
  2. customthe reaction at −78° C
  3. stirringAfter being stirred at room temperature for 1 h
  4. filtrationThe solid was filtered off
  5. washwashed with EtOAc
  6. customThe combined filtrate was partitioned
  7. extractionextracted with EtOAc (3×50 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customThe residue was purified by silica gel chromatography
  11. washeluting with EtOAc/petroleum ether (1:10)