HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(4-fluoro-2-nitrophenyl)piperidin-3-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| Edukt | 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-3-piperidinol hydrochloride | HCID 69312995 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(4-fluoro-2-nitrophenyl)piperidin-3-ol | HCID 69310204 | — |
Reaktionsschritte
To the solution of 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-3-piperidinol hydrochloride (6.0 g) obtained in Step 4 of Example 76 in 50 ml of ethanol, were added 2,5-difluoronitrobenzene (3.7 ml) and triethylamine (4.8 ml). The reaction mixture was refluxed overnight and concentrated. The resulting yellow solid was filtered and dried to give 7.2 g of the titled compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07342027B2 |
| Quelldatensatz | uspto-grants-2008_03 |
| ORD ID | ord-32fe0a73494a4cc08c23ded731469b18 |
| Quellennotiz | uspto-grants-2008_03 |