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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089772생성일: 2026년 10월 26일

Formic Acid → Flosequinan

https://huagongshe.com/reaction/1089772

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물Acetic AnhydrideHCID 7918—
반응물Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)-HCID 10059700—
용매WaterHCID 962—
생성물FlosequinanHCID 4474062—

반응 단계

A mixture of acetic anhydride (66.0 ml) and formic acid (45.0 ml) was stirred and heated at 50°-60° under nitrogen for 2 hours and then cooled to ambient temperature. 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphinylethanone (69.0 g), prepared in a similar manner to that described in Example 1, was added slowly below 30° and the mixture stirred for a further 2 hours. The mixture was cooled in an ice/salt bath to 0° and water (500 ml) added whilst maintaining the temperature below 30°. The mixture was filtered and the filtrate cooled in an ice/salt bath to 0°. Toluene (100 ml) and aqueous sodium hydroxide solution (specific gravity 1.5; 140 ml) were added sequentially, again maintaining the temperature below 30°. The mixture was stirred for 30 minutes at ambient temperature and the product collected by filtration, washed with water (200 ml), toluene (3×50 ml) and hexane (2×50 ml) and then dried at 50° in vacuo to give 7-fluoro-1-methyl-3-methylsulphinyl-4-quinolone, m.p.228.5°-230.5° (53.7 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05079264
출처 데이터셋uspto-grants-1992_01
ORD IDord-bb0c9187cb1241bfbf02c4bcf2a1127c
출처 메모uspto-grants-1992_01