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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408047Generated: October 27, 2026

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

https://huagongshe.com/reaction/408047

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 numberUS08754230B2
Source datasetuspto-grants-2014_06
ORD IDord-d1178c98ee174d70bc654a2047a0995e
Source noteuspto-grants-2014_06