HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43824Erstellt: 24. Oktober 2026
Cesium carbonate → Methyl 3-(4-benzyloxycarbonylaminopiperidin-1-yl)benzoate
https://huagongshe.com/de/reaction/43824
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Methyl 3-bromobenzoate | HCID 12070 | — |
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 4-Cbz-aminopiperidine | HCID 1514304 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Methyl 3-(4-benzyloxycarbonylaminopiperidin-1-yl)benzoate | HCID 68405998 | 26,6% |
Reaktionsschritte
Methyl 3-bromobenzoate (230 mg, 1.07 mmol), palladium acetate (12 mg, 0.054 mmol), BINAP (133 mg, 0.214 mmol) and cesium carbonate (767 mg, 2.35 mmol) were added to a solution of benzyl piperidin-4-yl-carbamate obtained in Example (192b) (248 mg, 0.817 mmol) in 1,4-dioxane (10 mL) and N,N-dimethylformamide (2.5 mL), and the mixture was stirred at 100° C. for 20 hours. The reaction solution was cooled, diluted with ethyl acetate, and washed with brine. The organic layer was dried over magnesium sulfate, and then the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/1) to obtain 80 mg of the title compound as a colorless oily substance (20%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536197B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-2d442424469f4ef68a66b1df757b2b4d |
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| Quellennotiz | uspto-grants-2013_09 |
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