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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68158생성일: 2026년 10월 24일

Sodium Iodide → methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionate

https://huagongshe.com/ko/reaction/68158

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DimethylformamideHCID 6228—
반응물Methyl 3-mercaptopropionateHCID 18050—
반응물1-(2-Chloroethyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-oneHCID 58492557—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionateHCID 5849249675.2%

반응 조건

온도80 °C

반응 단계

1-(2-Chloroethyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one (3.5 g, 8.98 mmol), methyl 3-mercaptopropionate (1.19 g, 9.88 mmol), and sodium iodide (1.48 g, 9.88 mmol) were added to DMF (30 ml) and stirred at 80° C. for 5 hours. Water and ethyl acetate were added to the reaction mixture, followed by separation. The thus-obtained organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane). The purified product was concentrated to dryness under reduced pressure, giving a pale yellow powder of methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionate (3.2 g, yield: 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045108E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-ae0d3f04578741a88bffe5a0a1aebf30
출처 메모uspto-grants-2014_09