HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408047Erstellt: 24. Oktober 2026
1,2,3-Triazine → Ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylate
https://huagongshe.com/de/reaction/408047
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2,3-Triazine | HCID 123047 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Ethyl 4-(4-fluorophenyl)-3-oxobutanoate | HCID 10585213 | — |
| Katalysator | 1,2,3-Triazine | HCID 123047 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylate | HCID 66771917 | 83% |
Reaktionsschritte
To a solution of ethyl 4-(4-fluorophenyl)-3-oxobutanoate (4.6 g, 21 mmol) in absolute EtOH (45 mL) was added NaOEt solution (21% NaOEt solution in EtOH, 7.7 mL) and triazine (1.67 g, 21 mmol). The resulting mixture was heated to 85° C. for 1.5 h, cooled to room temperature and treated with an additional portion of triazine (0.08 g, 1 mmol) and NaOEt solution (21% NaOEt solution in EtOH, 0.4 mL). The reaction mixture was heated for an additional hour and concentrated in vacuo. The residue was treated with 1N HCl until the pH of the reaction was about 2. The precipitate was collected to give the desired ester intermediate, ethyl 5-(4-fluorophenyl )-4-oxo-1,4-dihydropyridine-3-carboxylate (4.5 g, 83%) as a yellow solid. MS (ESI+) m/z 262 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754230B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-d1178c98ee174d70bc654a2047a0995e |
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| Quellennotiz | uspto-grants-2014_06 |
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