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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193565Generated: October 31, 2026

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

https://huagongshe.com/reaction/2193565

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 numberUS08329911B2
Source datasetuspto-grants-2012_12
ORD IDord-c8b92a8b077c4fbeb7f41978c4b73d5d
Source noteuspto-grants-2012_12