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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380949Generated: October 28, 2026

1,2,3-Triazine → Ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2380949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-TriazineHCID 123047—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 4-(4-fluorophenyl)-3-oxobutanoateHCID 10585213—
Catalyst1,2,3-TriazineHCID 123047—
SolventEthanolHCID 702—
ProductEthyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylateHCID 6677191783%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of ethyl 4-(4-fluorophenyl)-3-oxobutanoate (4.6 g, 21 mmol) in absolute ethanol (45 mL) was added NaOEt solution (21% NaOEt solution in EtOH, 7.7 mL) and triazine (1.67 g, 21 mmol). The resulting mixture was heated to 85° C. for 1.5 h, cooled to room temperature and treated with an additional portion of triazine (0.08 g, 1 mmol) and NaOEt solution (21% NaOEt solution in EtOH, 0.4 mL). The reaction mixture was heated for an additional hour and concentrated in vacuo. The residue was treated with 1N HCl until the pH of the reaction was about 2. The precipitate was collected to give the desired ester intermediate, ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylate (4.5 g, 83%) as a yellow solid. MS (ESI+) m/z 262 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258118B2
Source datasetuspto-grants-2012_09
ORD IDord-b8a2fb99d73f4abc832ef25d4d641f88
Source noteuspto-grants-2012_09