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HRID 408047作成日:2026年10月25日

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

https://huagongshe.com/reaction/408047

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3-TriazineHCID 123047—
反応物Sodium ethoxideHCID 2723922—
反応物Ethyl 4-(4-fluorophenyl)-3-oxobutanoateHCID 10585213—
触媒1,2,3-TriazineHCID 123047—
溶媒EthanolHCID 702—
生成物Ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylateHCID 6677191783%

反応条件

温度85 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754230B2
出典データセットuspto-grants-2014_06
ORD IDord-d1178c98ee174d70bc654a2047a0995e
出典メモuspto-grants-2014_06