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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486272생성일: 2026년 10월 23일

Diethyl (ethoxymethylene)malonate → diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate

https://huagongshe.com/ko/reaction/486272

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl (ethoxymethylene)malonateHCID 6871—
반응물3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylanilineHCID 18974495—
생성물diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonateHCID 19418744—

반응 조건

온도150 °C

반응 단계

To 3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline (1.57 g) is added diethyl ethoxymethylenemalonate (1.45 ml) and the mixture is heated at 150° C. for 25 hours. After cooling, the reaction product is purified by silica-gel column-chromatography (dichloromethane : methanol=100:1) to give diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]aminomethylene]malonate (1.50 g). The product is dissolved in acetic anhydride (7.9 ml) and thereto conc. sulfuric acid (3.16 ml) is added dropwise at 50°-60° C., followed by stirring for 30 minutes. The resultant mixture is poured into ice-water, neutralized, extracted with dichloromethane and the extract is dried The solvent is distilled off under reduced pressure. Purification by silica-gel column-chromatography (dichloromethane: methanol=10:1) to give ethyl 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate (26 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05290934
출처 데이터셋uspto-grants-1994_03
ORD IDord-950b467a75a04327b2e9a3a90f18be1a
출처 메모uspto-grants-1994_03