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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645423Generated: November 3, 2026

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

https://huagongshe.com/reaction/1645423

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 numberUS08124768B2
Source datasetuspto-grants-2012_02
ORD IDord-ff2b32043a6a4fdebfc8c4ed10777216
Source noteuspto-grants-2012_02