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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 967837생성일: 2026년 10월 26일

4-Chlorobenzenesulfonamide → 4-chloro-N-{[(2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamide

https://huagongshe.com/reaction/967837

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzenesulfonamideHCID 66824—
반응물phenyl 2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethylcarbamateHCID 22291420—
생성물4-chloro-N-{[(2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamideHCID 22291409—

반응 단계

The title compound was prepared according to the procedure described in step 2 of Example 18 from phenyl 2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethylcarbamate and 4-chlorobenzenesulfonamide. MS (ESI) m/z 527 [M+H]+, 525 [M−H]−, 1H-NMR (CDCl3) δ 1.24 (3H, t, J=7.5 Hz), 2.69 (2H, q, J=7.5 Hz), 2.83-2.90 (2H, m), 3.45-3.54 (2H, m), 6.50 (1H, br), 7.05 (2H, t, J=8.8 Hz), 7.18 (1H, s), 7.22-7.30 (2H, m), 7.42-7.52 (3H, m), 7.70-7.79 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956050B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-e25a5811901f428992744298d6ac8144
출처 메모uspto-grants-2005_10