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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239837생성일: 2026년 10월 26일

4-Methoxybenzenesulfonyl chloride → N-(2-benzoyl-4-bromo-phenyl)-4-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/239837

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzenesulfonyl chlorideHCID 7401—
반응물2-Amino-5-bromobenzophenoneHCID 99677—
생성물N-(2-benzoyl-4-bromo-phenyl)-4-methoxy-benzenesulfonamideHCID 9955192—

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)-phenyl-methanone and 103 mg of 4-Methoxy-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 3.78 (s, 3H), 6.83 (d, 2H, J=9.2 Hz), 7.39 (b, 1H), 7.49 (d, 2H, J=6.4 Hz), 7.68 (m, 4H), 8.85 (d, 2H, J=6.0 Hz), 9.96 (b, 1H). MS: m/z 447.0 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642808B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-39a15ca559334bffbb7439747cde7be0
출처 메모uspto-grants-2014_02