HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2518Erstellt: 23. Oktober 2026
Pyridine → 4-Trifluoroacetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide
https://huagongshe.com/de/reaction/2518
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide | HCID 19690071 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Trifluoroacetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide | HCID 19689922 | 81,2% |
Reaktionsschritte
4-Amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide (229.3 mg, 0.51 mmol) was dissolved in methylene chloride (2.0 ml) to which were subsequently added pyridine (0.05 ml, 0.62 mmol) and anhydrous trifluoroacetic acid (0.09 ml, 0.64 mmol) at 0° C. After 3 hours of stirring at 0° C. to room temperature, the reaction solution was mixed with saturated sodium bicarbonate aqueous solution and extracted with chloroform. The resulting organic layer was washed with saturated sodium chloride aqueous solution and water in that order, and dried on anhydrous sodium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol=20:1) to obtain 224.8 mg (81.2%) of the title compound in a light yellow powder form.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05728835 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-83156c93ebe44f9b836d2b41d4fbb6ea |
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| Quellennotiz | uspto-grants-1998_03 |
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