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HRID 2406作成日:2026年10月24日

Pyridine → N-(2-Methoxyphenyl)-3-pyridinesulfonamide

https://huagongshe.com/ja/reaction/2406

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-MethoxyanilineHCID 7000—
反応物Sodium CarbonateHCID 10340—
反応物Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物N-(2-Methoxyphenyl)-3-pyridinesulfonamideHCID 1968995883.5%

反応条件

温度100 °C

反応手順

o-Anisidine (377 mg, 3.0 mmol) was dissolved in toluene (10 ml) to which were subsequently added pyridine (0.48 ml, 6.0 mmol) and 3-pyridinesulfonylchloride hydrochloride (642 mg, 3.0 mmol) at room temperature. After 1.5 hours of stirring at 100° C., the resulting reaction solution was mixed with water (20 ml), adjusted to pH 7 to 8 with anhydrous sodium carbonate, extracted with ethyl acetate and then washed with water and saturated brine. After drying on anhydrous sodium carbonate and removing the solvent by evaporation, the resulting orange solid was purified by a silica gel column chromatography (ether:hexane=3:1) to obtain a light orange solid which was subsequently washed with an ether-hexane (1:3) mixture solution to obtain 662 mg (83.5%) of the title compound in the form of colorless prism crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728835
出典データセットuspto-grants-1998_03
ORD IDord-3ced4cee9a3c4c979b4e3a0eb0a11cbb
出典メモuspto-grants-1998_03