HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494403Erstellt: 25. Oktober 2026
Ethyl bromoacetate → [4-(4'-Trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl ester
https://huagongshe.com/reaction/494403
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | N-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamide | HCID 9928271 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | [4-(4'-Trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl ester | HCID 57683250 | — |
Reaktionsschritte
To a solution of 4-(4′-trifluoromethylbiphenyl-2-carbonylamino)piperidine (1.03 g) obtained in Example 8b) in dimethylformamide (5 mL) were added potassium carbonate (276 mg) and bromoacetic acid ethyl ester (223 μL). The mixture was stirred overnight at ambient temperature of 90° C., and then concentrated in vacuo. The residue was distributed with water and chloroform, and the aqueous layer was further extracted with chloroform. The organic layers were combined, washed with saturated brine, dried over sodium sulfate, concentrated in vacuo and purified by column chromatography on silica gel with chloroform:methanol=30:1 to give the title compound (598 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07538140B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-6f2ce5d29b81410d8be4796435f060ef |
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| Quellennotiz | uspto-grants-2009_05 |
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