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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

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzenesulfonyl chlorideHCID 7398—
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl methyl[(5-phenyl-1H-pyrrol-3-YL)methyl]carbamateHCID 57522146—
용매DimethylformamideHCID 6228—
생성물1-{1-[(4-Chlorophenyl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}-N-methylmethanamine hydrochlorideHCID 6692500666.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048909B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-0972bbf10e6b4890bb7b752e8b39f2b7
출처 메모uspto-grants-2011_11