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HRID 494403作成日:2026年10月26日

Ethyl bromoacetate → [4-(4'-Trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl ester

https://huagongshe.com/reaction/494403

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Potassium CarbonateHCID 11430—
反応物N-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamideHCID 9928271—
溶媒DimethylformamideHCID 6228—
生成物[4-(4'-Trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl esterHCID 57683250—

反応条件

温度90 °C

反応手順

To a solution of 4-(4′-trifluoromethylbiphenyl-2-carbonylamino)piperidine (1.03 g) obtained in Example 8b) in dimethylformamide (5 mL) were added potassium carbonate (276 mg) and bromoacetic acid ethyl ester (223 μL). The mixture was stirred overnight at ambient temperature of 90° C., and then concentrated in vacuo. The residue was distributed with water and chloroform, and the aqueous layer was further extracted with chloroform. The organic layers were combined, washed with saturated brine, dried over sodium sulfate, concentrated in vacuo and purified by column chromatography on silica gel with chloroform:methanol=30:1 to give the title compound (598 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07538140B2
出典データセットuspto-grants-2009_05
ORD IDord-6f2ce5d29b81410d8be4796435f060ef
出典メモuspto-grants-2009_05