HRID267015

反应详情

EQUATION

反应方程式

HRID 267015 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of ethyl 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propionate (3.21 g, 10 mmol) in tetrahydrofuran (THF, 100 ml), was added methylmagnesium bromide (10 ml, 30 mmol, 3M solution in ether) dropwise over 15 minutes at room temperature under N2. The resulting mixture was stirred for 16 hours. The mixture was slowly hydrolyzed with aqueous NH4Cl solution. The THF solution was diluted with EtOAc (300 ml), then was washed with water and brine. The organic solution was separated and dried over MgSO4. After removal of solvent, the crude product was purified by flash chromatography (25 g, SiO2 ; eluted with 1 CH3OH:99 DCM). The material thus purified weighed 2.36 g (77%) as white crystals. This was converted to the fumarate salt by treatment with fumaric acid (895 mg) in ethanol. Recrystallization from ethanol yielded white crystals, 2.47 g, m.p.=156°-158° C.

WORKUP

后处理

  1. washwas washed with water and brine
  2. customThe organic solution was separated
  3. dry with materialdried over MgSO4
  4. customAfter removal of solvent
  5. customthe crude product was purified by flash chromatography (25 g, SiO2 ; eluted with 1 CH3OH:99 DCM)
  6. customThe material thus purified
  7. customRecrystallization from ethanol yielded white crystals, 2.47 g, m.p.=156°-158° C.