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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Procainamide Hydrochloride | HCID 66068 | — |
| 反応物 | Phenylmethanesulfonyl chloride | HCID 74740 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | N-[4-[[2-(Diethylamino)ethyl]aminocarbonyl]phenyl]benzenemethanesulfonamide hydrochloride | HCID 20225361 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04544654 |
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| 出典データセット | uspto-grants-1985_10 |
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| ORD ID | ord-f2d5329eb79545eb9e5c139f863456b0 |
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| 出典メモ | uspto-grants-1985_10 |
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