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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230488생성일: 2026년 10월 24일

2,5-Dimethoxybenzenesulfonyl chloride → 2,5-Dimethoxy-N-[2-[(phenylsulfonyl)amino]4-(1-piperazinyl)phenyl]benzenesulfonamide

https://huagongshe.com/ko/reaction/230488

반응식

참여 물질

역할이름HCID투입량
반응물2,5-Dimethoxybenzenesulfonyl chlorideHCID 137025—
반응물N-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
생성물2,5-Dimethoxy-N-[2-[(phenylsulfonyl)amino]4-(1-piperazinyl)phenyl]benzenesulfonamideHCID 10302090—

반응 단계

2,5-Dimethoxy-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide was synthesized from of N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and 2,5-dimethoxybenzenesulfonylchloride (57 mg, 0.239 mmol) according to general method 3 to give 60 mg of a purple solid. MS (posES-FIA) m/z=Found: 533.1; Calcd: 533.14; 1H-NMR δ 7.68-7.48 (m, 5H), 7.16-7.05 (m, 4H), 6.69 (dd, 1H), 6.42 (d, 1H), 4.03 (s, 3H), 3.69 (s, 3H), 3.26-3.10 (m, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566715B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-c7e1de708b734e6b98662cffa745cfb1
출처 메모uspto-grants-2009_07