HRID1026001

反应详情

EQUATION

反应方程式

HRID 1026001 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4-(4-Chloro-phenyl)-5-(2,2,2-trifluoro-ethoxy)-pyridine-2-carboxylic acid (100 mg, 0.3 mmol, example D) was dissolved in dimethylformamide (4 mL). To this stirred solution under argon was added in sequence 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (107 mg, 0.3 mmol), N,N-diisopropyl ethyl amine (0.26 mL, 1.5 mmol) and 3-methoxy-5-isoxazolemethanamine hydrochloride (55 mg, 0.3 mmol). The mixture was shaken for 16 h at room temperature, solvent was removed in vacuo (45° C.) and the residue was digested with dichloromethane (5 mL) and 2N NaOH (1.5 mL) for 5 min. The mixture was absorbed onto 10 g ChemElut (Varian) and eluted with dichloromethane (70 mL). Solvent was evaporated and the brown, oily residue (160 mg) was purified by gradient chromatography on silica with ethyl acetate/n-heptane to give the title compound as a white solid (122 mg, 92%), LC-MS (UV peak area/ESI) 93%, 442.0769 (M+H)+.

WORKUP

后处理

  1. customsolvent was removed in vacuo (45° C.)
  2. waitthe residue was digested with dichloromethane (5 mL) and 2N NaOH (1.5 mL) for 5 min
  3. customThe mixture was absorbed onto 10 g ChemElut (Varian)
  4. washeluted with dichloromethane (70 mL)
  5. customSolvent was evaporated
  6. customthe brown, oily residue (160 mg) was purified by gradient chromatography on silica with ethyl acetate/n-heptane