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HRID 1089772作成日:2026年10月27日

Formic Acid → Flosequinan

https://huagongshe.com/reaction/1089772

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Acetic AnhydrideHCID 7918—
反応物Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)-HCID 10059700—
溶媒WaterHCID 962—
生成物FlosequinanHCID 4474062—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05079264
出典データセットuspto-grants-1992_01
ORD IDord-bb0c9187cb1241bfbf02c4bcf2a1127c
出典メモuspto-grants-1992_01