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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68173생성일: 2026년 10월 25일

Benzyloxyacetyl chloride → 1-(2-benzyloxyacetyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one

https://huagongshe.com/reaction/68173

반응식

참여 물질

역할이름HCID투입량
반응물Benzyloxyacetyl chlorideHCID 177085—
반응물Sodium BicarbonateHCID 516892—
반응물4-(Tert-butyldimethylsilyloxy)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-quinolinHCID 67417046—
용매DichloromethaneHCID 6344—
생성물1-(2-benzyloxyacetyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-oneHCID 5849236315%

반응 단계

Benzyloxyacetyl chloride (1.9 ml, 3 equivalent weight) was added to a dichloromethane solution (50 ml) of 4-(tert-butyldimethylsilyloxy)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-quinolin (1.5 g, 3.4 mmol) while ice-cooling and the mixture was stirred overnight at room temperature. An aqueous sodium bicarbonate solution was added to the reaction mixture, followed by extraction using ethyl acetate. The thus-obtained organic layer was dried over sodium sulfate, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=2:1). The purified product was concentrated under reduced pressure, giving a colorless oily substance of 1-(2-benzyloxyacetyl)-5-fluoro -3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one (250 mg, yield: 15%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045108E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-72e64c8d365e48549dc92681a5cbe5fa
출처 메모uspto-grants-2014_09