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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050855Generated: October 30, 2026

Pyridine → Ethyl 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1050855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantEthyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 53393185—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 6873591395%

Reaction Steps

A mixture of ethyl 4-ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate (60 g, 0.284 mol), 4-fluoro phenylboronic acid (120 g, 0.853 mol), Cu(OAc)2 (113 g, 0.568 mol) and pyridine (88 g, 1.137 mol) in DCM (500 mL) was stirred at RT for 4 h open to air. The reaction mixture was filtered and the solids were washed with water. The filtrate was extracted with DCM (2×250 mL). The combined organics were dried over Na2SO4 and concentrated to afford ethyl 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate. The product was carried forward without further purification. (77 g, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09387202B2
Source datasetuspto-grants-2016_07
ORD IDord-46d310946e854471be080e1a3d3e96b7
Source noteuspto-grants-2016_07