HRID931386

反应详情

EQUATION

反应方程式

HRID 931386 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

An ice-cold solution of 5-(hydroxymethyl)-N,N-dimethylfuro[2,3-b]pyridine-2-carboxamide (4.2 g, 0.019 mol) in DMF (15 mL) was added dropwise to a suspension of sodium hydride (60% dispersion in mineral oil, 1.14 g, 0.0286 mol) in DMF (15 mL) at 0° C. After the resulting mixture was stirred at 0° C. for 15 min, 4-methoxybenzyl chloride (3.89 g, 286 mmol) was added. The reaction mixture was gradually warmed to 23° C., and stirred for 1 h. The excess of sodium hydride was carefully quenched with water (15 mL). The reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by flash chromatography on silcia gel eluting with 35% ethyl acetate in petroleum ether to give the title compound. MS: m/z=341.2 (M+1).

WORKUP

后处理

  1. temperatureThe reaction mixture was gradually warmed to 23° C.
  2. stirringstirred for 1 h
  3. customThe excess of sodium hydride was carefully quenched with water (15 mL)
  4. extractionThe reaction mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography on silcia gel
  9. washeluting with 35% ethyl acetate in petroleum ether