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HRID 463678作成日:2026年10月26日

Procainamide Hydrochloride → N-[4-[[2-(Diethylamino)ethyl]aminocarbonyl]phenyl]benzenemethanesulfonamide hydrochloride

https://huagongshe.com/reaction/463678

反応式

関与物質

役割名称HCID仕込み量
反応物Procainamide HydrochlorideHCID 66068—
反応物Phenylmethanesulfonyl chlorideHCID 74740—
溶媒AcetoneHCID 180—
生成物N-[4-[[2-(Diethylamino)ethyl]aminocarbonyl]phenyl]benzenemethanesulfonamide hydrochlorideHCID 20225361—

反応条件

温度-50 °C

反応手順

To a solution of 7.1 g (0.026 moles) of procainamide hydrochloride in 100 ml acetone and 5 ml triethylamino at -50° C., is added slowly 5.0 g (0.026 moles) of α-toluenesulfonyl chloride. Stir at -50° C. for 1 hour, then warm to room temperature and stir for 16 hours. Remove the solvent in vacuo. Slurry the residue in 200 ml ether, and wash 2×100 ml portions of methylene chloride. The combined methylene chloride extracted are vacuum stripped to dryness. The residue is dissolved in 100 ml ethanol and brought to pH 3 with concentrated hydrochloric acid. The solvent is removed in vacuo, and the residue triturated with methylene-chloride to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04544654
出典データセットuspto-grants-1985_10
ORD IDord-f2d5329eb79545eb9e5c139f863456b0
出典メモuspto-grants-1985_10