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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195527Generated: November 2, 2026

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

https://huagongshe.com/reaction/2195527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantMethyl 2-oxo-1,2-dihydropyridine-3-carboxylateHCID 579028—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 21081723100%

Reaction Steps

To a mixture of methyl 2-oxo-1,2-dihydropyridine-3-carboxylate (6.0 g, 39 mmol), 4-fluorophenylboronic acid (16.3 g, 116 mmol), cupric acetate (14 g, 78 mmol) and pyridine (12 g, 0.156 mol) in DCM (300 mL) is added 4 Å molecular sieves (5 g). The reaction mixture is stirred at RT overnight open to air. After the solids are filtered and washed with water, the filtrate is extracted with DCM (100 mL). The organic layer is dried over MgSO4 and concentrated. The residue is purified by silica gel column chromatography eluting with PE:DCM (2:1 to 0:1) to give the product (9.6 g, 100% yield). MS (m/z): 248.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043878E1
Source datasetuspto-grants-2012_12
ORD IDord-5ef73f7684884295b7d5174c40d8a85d
Source noteuspto-grants-2012_12