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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktEthyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 247443—
Edukt4-Fluorophenylboronic acidHCID 285645—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl 1-(4-fluorophenyl)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 6676711916,6%

Reaktionsbedingungen

Temperatur80 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030302B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-6cf3d172ad5f4598a06a58d9bc8a9698
Quellennotizuspto-grants-2011_10