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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043052Generated: October 27, 2026

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

https://huagongshe.com/reaction/1043052

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 EtOH (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 numberUS08558000B2
Source datasetuspto-grants-2013_10
ORD IDord-eacbce79c2584391bc194b20f5def4b8
Source noteuspto-grants-2013_10