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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13857Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/13857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3-bromopropanoateHCID 76934—
EduktDiisopropylethylamineHCID 81531—
EduktBiphenyl-2-ylcarbamic Acid Piperidin-4-yl EsterHCID 10851461—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionateHCID 5745943670%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728144B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d5ce28f4093644dea52f9b79850cc92e
Quellennotizuspto-grants-2010_06