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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13857생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/13857

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-bromopropanoateHCID 76934—
반응물DiisopropylethylamineHCID 81531—
반응물Biphenyl-2-ylcarbamic Acid Piperidin-4-yl EsterHCID 10851461—
용매AcetonitrileHCID 6342—
생성물Methyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionateHCID 5745943670%

반응 조건

온도50 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728144B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d5ce28f4093644dea52f9b79850cc92e
출처 메모uspto-grants-2010_06