HRID1987224

反应详情

EQUATION

反应方程式

HRID 1987224 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

N-(4-Fluoro-3-nitrophenyl)ethanesulfonamide (26 g, 0.107 mol), [(4,4-difluorocyclohexyl)methyl]amine (approx. 15 g), DIPFA (20 mL) and DMSO (100 mL) were mixed together and heated to 65° C. overnight. Ethanolamine (5 g) was added and the reaction mixture was stirred until complete disappearance of N-(4-fluoro-3-nitrophenyl)ethanesulfonamide (approx. 4-5 hrs.). The room temperature cooled down reaction mixture was poured in cold water (900 mL). The product was extracted with DCM (5×200 mL). The combined organic phases were washed with HCl 2N (3×200 mL) and dried over anhydrous Na2SO4. The solvent was removed and the crude product was purified on silica gel by flash chromatography (this material can be re-crystallized using a mixture of EtOAc and hexane) to provide the title product (24.2 g) as orange solid.

WORKUP

后处理

  1. temperatureThe room temperature cooled down
  2. customreaction mixture
  3. extractionThe product was extracted with DCM (5×200 mL)
  4. washThe combined organic phases were washed with HCl 2N (3×200 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. customThe solvent was removed
  7. customthe crude product was purified on silica gel by flash chromatography (this material
  8. customcan be re-crystallized
  9. additiona mixture of EtOAc and hexane)