反应详情

To a solution of 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-2-hydroxyethyl]-methyl-amide (the compound of Preparation Example 48) (150 mg) in tetrahydrofuran (3 mL) and ethanol (3 mL) was added an aqueous solution (2.5 mL) of hydroxyamine hydrochloride (112 mg) and sodium acetate (133 mg), and the mixture was stirred at 70–80° C. for 3 hours. The organic solvent was removed by evaporation, water and ethyl acetate were added for separation/extraction. The organic layer was dried with anhydrous magnesium sulfate, the solvent was evaporated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate; ethyl acetate 10–40%). Among the 2 spots detected by TLC (the solvent system; hexane-ethyl acetate=1:1), the polar fractions (low Rf value on TLC) were collected, and the title compound (116 mg) was obtained as a colorless solid.

1. customThe organic solvent was removed by evaporation, water and ethyl acetate
2. additionwere added for separation/extraction
3. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
4. customthe solvent was evaporated
5. customthe residue was purified by silica gel column chromatography (hexane/ethyl acetate; ethyl acetate 10–40%)
6. customhexane-ethyl acetate=1:1), the polar fractions (low Rf value on TLC) were collected