HRID419102

反应详情

EQUATION

反应方程式

HRID 419102 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

To Fe power (2.18 g, 39.0 mmol), AcOH (10 mL) was added drop wise and heated to 80° C. To it, a solution of 2-bromo-5-methyl-3-nitro-pyridine (1.96 g, 9.07 mmol) in AcOH (10 mL) was added slowly. After 30 min, reaction mixture was allowed to cool to room temperature and diluted with EtOAc (25 mL), filtered through a pad of celite. The filter cake was washed with EtOAc (25 mL) and filterate was concentrated. The residual liquid was slowly treated with saturated aqueous NaHCO3 solution (70 mL), followed by small portions of solid NaHCO3 to neutralize the AcOH, extracted with EtOAc (2×50 mL) and the extracts were dried (anhydrous Na2SO4) and concentrated under reduced pressure to get 2-bromo-5-methyl-pyridin-3-ylamine (1.45 g) as a brown solid in 86.3% yield. ESMS m/z (relative intensity): 187 (M+H)+ (100).

WORKUP

后处理

  1. customreaction mixture
  2. temperatureto cool to room temperature
  3. filtrationfiltered through a pad of celite
  4. washThe filter cake was washed with EtOAc (25 mL) and filterate
  5. concentrationwas concentrated
  6. additionThe residual liquid was slowly treated with saturated aqueous NaHCO3 solution (70 mL)
  7. extractionextracted with EtOAc (2×50 mL)
  8. dry with materialthe extracts were dried (anhydrous Na2SO4)
  9. concentrationconcentrated under reduced pressure