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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29554생성일: 2026년 10월 23일

p-(Trifluoromethoxy)benzenesulphonyl chloride → N-[4-Bromo-2-(pyridine-4-carbonyl)-phenyl]4-trifluoromethoxy-benzenesulfonamide

https://huagongshe.com/ko/reaction/29554

반응식

참여 물질

역할이름HCID투입량
반응물p-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
반응물(2-Amino-5-bromophenyl)(pyridin-4-yl)methanoneHCID 13549724—
생성물N-[4-Bromo-2-(pyridine-4-carbonyl)-phenyl]4-trifluoromethoxy-benzenesulfonamideHCID 10413664—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 138 mg of (2-Amino-5-bromo-phenyl)-pyridin-4-yl-methanone and 130 mg of 4-trifluoromethoxy-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 7.21 (d, 2H, J=8.8 Hz), 7.35 (m, 2H), 7.45 (s,1H), 7.70 (m, 2H), 7.83 (m, 2H), 8.82 (dd, 2H, J=4.8 Hz, 1.6 Hz), 10.21 (s, 1H). MS: m/z 502.3 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-23ae0520035146ffafafc40366fc5199
출처 메모uspto-grants-2008_09