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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1006417생성일: 2026년 10월 26일

3,5-Dichlorobenzenesulfonyl chloride → 4-(4-benzyl-piperazin-1-yl)-1-(3,5-dichloro-benzenesulfonyl)-1H-indole

https://huagongshe.com/reaction/1006417

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dichlorobenzenesulfonyl chlorideHCID 522388—
반응물4-(4-Benzyl-piperazin-1-yl)-1H-indoleHCID 2728532—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Sodium HydroxideHCID 14798—
생성물4-(4-benzyl-piperazin-1-yl)-1-(3,5-dichloro-benzenesulfonyl)-1H-indoleHCID 12137124100.5%

반응 단계

4-(4-Benzyl-piperazin-1-yl)-1H-indole (274 mg, 0.94 mmole) and 50 mg tetra-n-butylammonium hydrogen sulfate was stirred in a mixture of 10 mL toluene and 5 mL 4 N sodium hydroxide. Solid 3,5-dichlorobenzenesulfonyl chloride (246 mg, 1.0 mmole) was added in one portion. The reaction mixture was stirred at room temperature for 6 hours, then it was diluted with 20 mL water and extracted with 25 mL ethyl acetate. The organic phase was washed with 10 mL saturated sodium chloride solution, dried (magnesium sulfate) and concentrated. Recrystallization from dichloromethane provided 473 mg of 4-(4-benzyl-piperazin-1-yl)-1-(3,5-dichloro-benzenesulfonyl)-1H-indole, m.p. 201-203° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06790848B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-9c0ec165595848a990ab93ee514ccaec
출처 메모uspto-grants-2004_09