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HRID 13857作成日:2026年10月26日

Methyl 3-bromopropanoate → Methyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionate

https://huagongshe.com/reaction/13857

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-bromopropanoateHCID 76934—
反応物DiisopropylethylamineHCID 81531—
反応物Biphenyl-2-ylcarbamic Acid Piperidin-4-yl EsterHCID 10851461—
溶媒AcetonitrileHCID 6342—
生成物Methyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionateHCID 5745943670%

反応条件

温度50 °C

反応手順

Methyl 3-bromopropionate (553 μL, 5.07 mmol) was added to a stirred solution of biphenyl-2-ylcarbamic acid piperidin-4-yl ester (1.00 g, 3.38 mmol; prepared as described in Preparation 1) and DIPEA (1.76 mL, 10.1 mmol) in ACN (34 mL) at 50° C. and the reaction mixture was heated at 50° C. overnight. The solvent was then removed under reduced pressure, and the residue was dissolved in DCM (30 mL). The resulting solution was washed with saturated aqueous sodium bicarbonate solution (10 mL), dried over MgSO4, filtered and the solvent was removed under reduced pressure. The crude residue was purified by column chromatography (5-10% MeOH/DCM) to give 905 mg of the title intermediate (70% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728144B2
出典データセットuspto-grants-2010_06
ORD IDord-d5ce28f4093644dea52f9b79850cc92e
出典メモuspto-grants-2010_06