HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 4-(4-Fluorobenzoylamino)-1-methylsulfonylpiperidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 4-fluoro-N-(piperidin-4-yl)benzamide | HCID 4778226 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(4-Fluorobenzoylamino)-1-methylsulfonylpiperidine | HCID 5009999 | — |
Reaktionsschritte
To a solution of 4-(4-fluorobenzoylamino)piperidine (0.15 g) in dichloromethane (5 ml) were added in turn pyridine (0.14 ml) and methanesulfonyl chloride (96 μl) at 0° C. The mixture was allowed to warm to ambient temperature and stirred for 1 hour. To the mixture was added N,N-dimethylaminopyridine (0.13 g) and allowed to stir for another 1 hour. The reaction mixture was taken up into a mixture of water and dichloromethane. The separated organic layer was washed in turn with hydrochloric acid (1N), aqueous sodium hydrogen carbonate, and brine, and dried over magnesium sulfate. Evaporation under reduced pressure gave a residue, which was triturated with diisopropyl ether to give 4-(4-fluorobenzoylamino)-1-methylsulfonylpiperidine (0.30 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06710043B1 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-2f51fc0c5b304c23b768fa1289a84422 |
| Quellennotiz | uspto-grants-2004_03 |