HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1662019Erstellt: 24. Oktober 2026
Pyridine → Ethyl 1-(4-fluorophenyl)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate
https://huagongshe.com/de/reaction/1662019
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 247443 | — |
| Edukt | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Ethyl 1-(4-fluorophenyl)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 66767119 | 16,6% |
Reaktionsschritte
A suspension of ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate (5.0 g, 0.025 mol), 4-fluorophenylboronic acid (10.7 g, 0.077 mol), cupric acetate (1.33 g, 0.007 mol), pyridine (6.86 mL), and 4 A molecular sieves (5.0 g) in 1,4-dioxane (80 mL) is heated at 80° C. for 68 hours. The solids are filtered off and the filtrate is concentrated. The residue is partitioned with EtOAc (50 mL) and 2N HCl (70 mL). The precipitated solid is collected by filtration and washed with EtOAc to give the title product (1.2 g). The EtOAc filtrate is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:EtOAc:MeOH (40:20:1) to give another portion of product (0.12 g), (1.32 g total, 17.8% yield). MS (m/z): 290.1 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08030302B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-6cf3d172ad5f4598a06a58d9bc8a9698 |
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| Quellennotiz | uspto-grants-2011_10 |
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