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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2195541생성일: 2026년 10월 25일

Ammonium Chloride → Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2195541

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoateHCID 66767015—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 6676714362.5%

반응 조건

온도90 °C

반응 단계

A mixture of ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoate (1.85 g, 6.97 mmol) and N,N-dimethylformamide dimethyl acetal (5 mL, 37.45 mmol) is stirred at 90° C. for 90 min. After the reaction is cooled, EtOAc (30 mL) and saturated NH4Cl solution (20 mL) are added. The organic phase is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with DCM:MeOH (10:1). The fractions containing product are concentrated, and the residue is mixed with ether to give 1.2 g of yellow solid which is filtered and discarded. The filtrate is concentrated and purified again by silica gel column chromatography eluting with DCM:MeOH (20:1) to give the product (500 mg, 26% yield). MS (m/z): 276.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE043878E1
출처 데이터셋uspto-grants-2012_12
ORD IDord-0aa1cb2fe09842b09a49d36bdbea97aa
출처 메모uspto-grants-2012_12