HRID378936

反应详情

EQUATION

反应方程式

HRID 378936 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a room temperature, stirred mixture of (S)-3-(4-benzyloxy-phenyl)-2-[4-(4-phenyl-piperidin-1-yl)-benzenesulfonylamino]-propionic acid (0.033 g, 0.000058 mol) in thioanisole (0.34 mL) was added trifluoroacetic acid (1 mL), and the mixture was stirred for 18 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried (Na2SO4) and rotary-evaporated under reduced pressure to remove volatiles. The resulting yellow solution was chromatographed on silica gel (5.5 g) eluting with dichloromethane (10×5 mL) followed by dichloromethane-methanol (14:1). Fractions containing product were rotary-evaporated. The residue was suspended in water and stirred to give the title compound as an off-white solid; yield 0.0079 g (28%), mp 108-110° C.

WORKUP

后处理

  1. stirringthe mixture was stirred for 18 hours
  2. extractionextracted with ethyl acetate
  3. dry with materialThe organic layer was dried (Na2SO4)
  4. customrotary-evaporated under reduced pressure
  5. customto remove volatiles
  6. customThe resulting yellow solution was chromatographed on silica gel (5.5 g)
  7. washeluting with dichloromethane (10×5 mL)
  8. additionFractions containing product
  9. customwere rotary-evaporated
  10. stirringstirred