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HRID 2516作成日:2026年10月24日

Boron tribromide → 4-Acetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-hydroxyphenyl)benzamide

https://huagongshe.com/ja/reaction/2516

反応式

関与物質

役割名称HCID仕込み量
反応物Boron tribromideHCID 25134—
反応物Sodium BicarbonateHCID 516892—
反応物4-Acetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-methoxyphenyl)benzamideHCID 19689904—
溶媒DichloromethaneHCID 6344—
生成物4-Acetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-hydroxyphenyl)benzamideHCID 1968979876.7%

反応手順

4-Acetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-methoxyphenyl)benzamide (50.0 mg, 0.10 mmol) was dissolved in methylene chloride (3.0 ml) to which was subsequently added a methylene chloride solution (1 ml) of boron tribromide (0.018 ml, 0.19 mmol) at 0° C. After 12 hours of stirring at 0° C. to room temperature, the reaction solution was mixed with saturated sodium bicarbonate aqueous solution and extracted with ethyl acetate. The resulting organic layer was washed with saturated sodium bicarbonate aqueous solution and saturated brine, and dried on anhydrous sodium sulfate. Thereafter, the solvent was distilled off under a reduced pressure, and the resulting residue was purified by a silica gel column chromatography (ethyl acetate-chloroform:methanol=10:1) to obtain 37.3 mg (76.7%) of the title compound in a light yellow amorphous form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728835
出典データセットuspto-grants-1998_03
ORD IDord-afe5cbc25fd340cf8536ac9ee64ce538
出典メモuspto-grants-1998_03