Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 463678생성일: 2026년 10월 25일
Procainamide Hydrochloride → N-[4-[[2-(Diethylamino)ethyl]aminocarbonyl]phenyl]benzenemethanesulfonamide hydrochloride
https://huagongshe.com/reaction/463678
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Procainamide Hydrochloride | HCID 66068 | — |
| 반응물 | Phenylmethanesulfonyl chloride | HCID 74740 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | N-[4-[[2-(Diethylamino)ethyl]aminocarbonyl]phenyl]benzenemethanesulfonamide hydrochloride | HCID 20225361 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04544654 |
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| 출처 데이터셋 | uspto-grants-1985_10 |
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| ORD ID | ord-f2d5329eb79545eb9e5c139f863456b0 |
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| 출처 메모 | uspto-grants-1985_10 |
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