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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18889생성일: 2026년 10월 25일

2-Amino-5-chlorobenzophenone → N-(2-Benzoyl-4-chloro-phenyl)-4-methanesulfonyl-benzenesulfonamide

https://huagongshe.com/reaction/18889

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-chlorobenzophenoneHCID 12870—
반응물4-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735182—
생성물N-(2-Benzoyl-4-chloro-phenyl)-4-methanesulfonyl-benzenesulfonamideHCID 11408313—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 115 mg of (2-amino-5-chloro-phenyl)-phenyl-methanone and 127 mg of 4-Methanesulfonyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 2.92 (s, 3H), 7.34 (m, 3H), 7.434 (m, 2H), 7.51 (dd, 1H, J=8.8 Hz, 2.4 Hz), 7.60 (m, 1H), 7.75 (d, 1H, J=8.8 Hz), 7.80-7.86 (m, 4H), 9.86 (b, 1H). MS: m/z 450.9 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741519B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4fd6963b18fb454382e486e6af2332c3
출처 메모uspto-grants-2010_06