Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554401생성일: 2026년 10월 25일
4-Chlorobenzenesulfonyl chloride → 1-{1-[(4-Chlorophenyl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride
https://huagongshe.com/reaction/554401
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Tert-butyl methyl[(5-phenyl-1H-pyrrol-3-YL)methyl]carbamate | HCID 57522146 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-{1-[(4-Chlorophenyl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride | HCID 66925006 | 66.8% |
반응 단계
To a solution (7 mL) of tert-butyl methyl[(5-phenyl-1H-pyrrol-3-yl)methyl]carbamate (70 mg) in N,N-dimethylformamide was added sodium hydride (60% in oil, 13 mg) and the mixture was stirred for 30 min. 4-Chlorobenzenesulfonyl chloride (62 mg) was added at room temperature and the mixture was stirred for 1 hr. To the reaction mixture was added ice water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→4:1), and dissolved in methanol (10 mL). 4 mol/L Hydrogen chloride-ethyl acetate solution (1.5 mL) was added and the mixture was stirred at 65° C. for 30 min. The reaction mixture was concentrated under reduced pressure, and crystallized from ethyl acetate to give the title compound as pale-red crystals (yield 39 mg, 40%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08048909B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-0972bbf10e6b4890bb7b752e8b39f2b7 |
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| 출처 메모 | uspto-grants-2011_11 |
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