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HRID 408047생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/408047

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3-TriazineHCID 123047—
반응물Sodium ethoxideHCID 2723922—
반응물Ethyl 4-(4-fluorophenyl)-3-oxobutanoateHCID 10585213—
촉매1,2,3-TriazineHCID 123047—
용매EthanolHCID 702—
생성물Ethyl 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylateHCID 6677191783%

반응 조건

온도85 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754230B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-d1178c98ee174d70bc654a2047a0995e
출처 메모uspto-grants-2014_06