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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 967836생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/967836

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorobenzenesulfonamideHCID 81410—
반응물phenyl 2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethylcarbamateHCID 22291420—
생성물2-chloro-N-{[(2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamideHCID 22291413—

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 2-chlorobenzenesulfonamide. MS (ESI) m/z 527 [M+H]+, 525 [M−H]−, 1H-NMR (CDCl3)δ1.25 (3H, t, J=7.5 Hz), 2.71 (2H, q, J=7.5 Hz), 2.85 (2H, t, J=7.0 Hz), 3.47-3.54 (2H, m), 6.57 (1H, br), 7.07 (2H, t, J=8.8 Hz), 7.19 (1H, s), 7.26 (2H, s), 7.40-7.46 (1H, m), 7.57-7.61 (2H, m), 7.73-7.78 (2H, m), 8.00 (2H, d, J=7.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956050B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-723338fa39a047d3bc343c2f60528e41
출처 메모uspto-grants-2005_10