HRID29882

反应详情

EQUATION

反应方程式

HRID 29882 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a mixture of N-Boc piperidine-4-carboxylic acid (9.2 g, 0.04 mol) and DCC (dicyclohexylcarbodiimide) (8.2 g, 0.04 mol) in ethyl acetate (150 mL) was added HOAt (1-hydroxy-7-azabenzotriazole) (5.5 g, 0.04 mol) in DMF (dimethylformamide) (40 mL). The mixture was stirred at room temperature for 10 minutes and then 3-(4-fluoro-phenoxy)-phenylamine (8.7 g, 0.043 mol) in ethyl acetate (50 mL) was added. The reaction mixture was allowed to stir overnight at room temperature and then was concentrated to remove most of the ethyl acetate. The precipitated solid was removed by filtration through Celite. The filtrate was diluted with ethyl acetate and washed with 1 N HCl, saturated NaHCO3 and brine (3×60 mL). The organic phase was dried with MgSO4 and concentrated. The residue was purified on silica eluting with 20% ethyl acetate/hexanes to afford 4-[3-(4-fluoro-phenoxy)-phenylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (14.2 g, 86%) as an off-white solid.

WORKUP

后处理

  1. stirringto stir overnight at room temperature
  2. concentrationwas concentrated
  3. customto remove most of the ethyl acetate
  4. customThe precipitated solid was removed by filtration through Celite
  5. additionThe filtrate was diluted with ethyl acetate
  6. washwashed with 1 N HCl, saturated NaHCO3 and brine (3×60 mL)
  7. dry with materialThe organic phase was dried with MgSO4
  8. concentrationconcentrated
  9. customThe residue was purified on silica eluting with 20% ethyl acetate/hexanes