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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29604생성일: 2026년 10월 24일

4-Methanesulfonylbenzene-1-sulfonyl chloride → N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-methanesulfonyl-benzenesulfonamide

https://huagongshe.com/ko/reaction/29604

반응식

참여 물질

역할이름HCID투입량
반응물4-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735182—
반응물(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanoneHCID 22327305—
생성물N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-methanesulfonyl-benzenesulfonamideHCID 10367205—

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 )-(6-methyl-pyridin-3-yl )-methanone and 4-Methanesulfonyl-benzenesulfonyl chloride and purified by HPLC. 1H NMR (CDCl3) δ 9.77 (br s, 1H, NH), 8.44 (dm, 1H, J=2.2 Hz), 7.87 (d, 2H, J=8.8 Hz), 7.83 (d, 2H, J=8.8 Hz), 7.76 (d, 1H, J=8.8 Hz), 7.60 (dd, 1H, J=8.0 Hz, J=2.2 Hz), 7.55 (dd, 1H, J=8.8 Hz, J=2.2 Hz), 7.36 (d, 1H, J=2.2), 7.26 (d, 1H, J =8.0 Hz), 3.00 (s, 3H), 2.66 (s, 3H). MS: m/z 465 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-aaca2cfc13a44b3e9a31abe4a4bdd34a
출처 메모uspto-grants-2008_09