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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510613Generated: October 26, 2026

Ethyl Acrylate → 7-Fluoro-1,5-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/1510613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
Reactant2-Bromo-5-fluoropyridin-3-amineHCID 40427367—
CatalystHCID 178418851HCID 178418851—
SolventTriethylamineHCID 8471—
Product7-Fluoro-1,5-naphthyridin-2(1H)-oneHCID 46900801—
Productethyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylateHCID 68105283—

Reaction Conditions

Temperature147.5 °C

Reaction Steps

To 0.99 g of 2-bromo-5-fluoropyridin-3-amine, 0.67 mL of ethyl acrylate, 3.5 mL of triethylamine, and 0.13 g of bis(tri-tert-butylphosphine)palladium(0) were added, and the mixture was stirred at an external temperature of 145 to 150° C. for 5 hours in a sealed tube. The reaction mixture was cooled to room temperature and the solvent was distilled off under reduced pressure. The resultant residue was purified by flash silica gel column chromatography using gradient elution with chloroform:methanol=100:0 to 90:10 to obtain 0.37 g of ethyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate and 0.15 g of 7-fluoro-1,5-naphthyridin-2(1H)-one as light brown solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211908B2
Source datasetuspto-grants-2012_07
ORD IDord-5f9e88e7673d4358b8e829909d845ee2
Source noteuspto-grants-2012_07