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HRID 248752作成日:2026年10月24日

Pyridine → 4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acid

https://huagongshe.com/ja/reaction/248752

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Sodium HydroxideHCID 14798—
反応物4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
反応物4-(Chlorosulfonyl)benzoic acidHCID 82385—
溶媒DichloromethaneHCID 6344—
生成物4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acidHCID 3699990—

反応手順

10 g (55.8 mmol) of 4-fluoro-3-trifluoromethylaniline and 6 ml (74.3 mmol) of pyridine are dissolved in 250 ml of dichloromethane. The mixture is cooled with ice water and, under agitation and exclusion of moisture, 12.7 g (57.6 mmol) of 4-chlorosulfonylbenzoic acid is added in incremental portions. The mixture is stirred overnight; the slurry is combined with 75 ml of 2N sodium hydroxide solution, and the organic phase is separated. The alkaline solution is washed with dichloromethane and then adjusted to pH 2 with hydrochloric acid. The product is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulfate and concentrated to dryness. The title compounds melts at 243-°245° C. after crystallization from ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210290
出典データセットuspto-grants-1993_05
ORD IDord-b639f8a2c482415fbde171d119d57f67
出典メモuspto-grants-1993_05