反应详情

In DMF (5 ml), 2-(2-methylphenylamino)-5-benzoxazolylacetic acid (282 mg, 1.0 mmol), methyl 4-((2S,4S)-4-fluoro-1-2-pyrrolidinylmethoxy)benzoate (253 mg, 1.0 mmol), EDC•HCl (288 mg, 1.5 mmol), HOBT (203 mg, 1.5 mmol) and triethylamine (0.70 ml, 5.0 mmol) were stirred at room temperature for 18 hours. The reaction mixture was poured in water, followed by extraction with ethyl acetate. The extract was washed with ice water and saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (silica gel: 50 g), whereby from chloroform/acetone (10/1) eluate fractions, the title compound (405 mg, 78%) was obtained as a pale brown amorphous substance.

1. extractionfollowed by extraction with ethyl acetate
2. washThe extract was washed with ice water and saturated brine
3. dry with materialdried over anhydrous sodium sulfate
4. distillationdistilled under reduced pressure
5. customto remove the solvent
6. customThe residue was purified by chromatography on a silica gel column (silica gel: 50 g), whereby from chloroform/acetone (10/1) eluate fractions