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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29591생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/29591

반응식

참여 물질

역할이름HCID투입량
반응물p-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
반응물(2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanoneHCID 22327293—
생성물N-[4-Chloro-2-(2-methyl-pyridine-4-carbonyl)-phenyl]-4-trifluoromethoxy-benzenesulfonamideHCID 10254154—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanone and 4-trifluoromethoxy-benzenesulfonyl chloride and purified by HPLC. 1H NMR (CDCl3) δ 10.17(s, 1H) 8.63 (d, J=4 Hz, 1H) 7.78 (m, 3H) 7.51 (s, 1H) 7.30 (s, 1H) 7.17 (s, 1H) 7.09 (s, 1H) 6.97 (d, J=4 Hz, 2H) 2.64 (s, 3H). MS (ES) m/z=471.0 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-62f889d800ca41bc9c140d0a1f465a24
출처 메모uspto-grants-2008_09