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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989829Generated: November 3, 2026

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

https://huagongshe.com/reaction/1989829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-bromopropanoateHCID 76934—
ReactantDiisopropylethylamineHCID 81531—
ReactantBiphenyl-2-ylcarbamic Acid Piperidin-4-yl EsterHCID 10851461—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionateHCID 5745943670%

Reaction Conditions

Temperature50 °C

Reaction Steps

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 (magnesium sulfate), 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642355B2
Source datasetuspto-grants-2010_01
ORD IDord-5fe002b0e6da41a6967d40c25e48cb7e
Source noteuspto-grants-2010_01