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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346745생성일: 2026년 10월 25일

2,1,3-Benzoxadiazole-4-sulfonyl chloride → N-(2,1,3-benzoxadiazol-4-yl)-4-(1,4-diazepan-1-yl)-2-[(phenylsulfonyl)amino]benzenesulfonamide hydrochloride

https://huagongshe.com/reaction/346745

반응식

참여 물질

역할이름HCID투입량
반응물2,1,3-Benzoxadiazole-4-sulfonyl chlorideHCID 2735446—
반응물N-(2-amino-5-(4-t-butyloxycarbonyl-1,4-diazepan-1-yl)-phenyl}benzenesulfonamideHCID 22272501—
생성물N-(2,1,3-benzoxadiazol-4-yl)-4-(1,4-diazepan-1-yl)-2-[(phenylsulfonyl)amino]benzenesulfonamide hydrochlorideHCID 22272516—

반응 단계

N-(2,1,3-benzoxadiazol-4-yl)-4-(1,4-diazepan-1-yl)-2-[(phenylsulfonyl)amino]benzenesulfonamide hydrochloride was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-1,4-diazepan-1-yl)-phenyl}benzenesulfonamide (0.072 g, 0.16 mmol) and 2,1,3-benzoxadiazol-4-yl sulfonyl chloride (0.072 g, 0.21 mmol) to give 38.0 mg of a light purple solid; M+1 537.2 Calcd 537.15; 1HNMR δ 8.21 (d, 1H), 7.80 (d, 1H), 7.68–7.46 (m, 6H), 6.92 (d, 1H), 6.49 (dd, 1H), 6.12 (d, 1H), 3.57 (app t, 2H), 3.34 (app t, 2H), 3.17 (app t, 2H), 3.11 (app t, 2H), 2.03–1.95 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173035B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-b48e57c4565c453f883b1d3431696ea3
출처 메모uspto-grants-2007_02