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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl 3-bromopropanoate | HCID 76934 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Biphenyl-2-ylcarbamic Acid Piperidin-4-yl Ester | HCID 10851461 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Methyl 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionate | HCID 57459436 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728144B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-d5ce28f4093644dea52f9b79850cc92e |
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| Quellennotiz | uspto-grants-2010_06 |
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