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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29571생성일: 2026년 10월 23일

4-t-Butylbenzenesulfonyl chloride → 4-tert-Butyl-N-[4-chloro-2-(pyridine-2-carbonyl)-phenyl]-benzenesulfonamide

https://huagongshe.com/ko/reaction/29571

반응식

참여 물질

역할이름HCID투입량
반응물4-t-Butylbenzenesulfonyl chlorideHCID 139882—
반응물(2-Amino-5-chlorophenyl)(pyridin-2-yl)methanoneHCID 288049—
생성물4-tert-Butyl-N-[4-chloro-2-(pyridine-2-carbonyl)-phenyl]-benzenesulfonamideHCID 10094123—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 116 mg of (2-Amino-5-chloro-phenyl)-pyridin-2-yl-methanone and 116 mg of 4-tert-Butyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 1.24 (s, 9H), 7.34-7.38 (m, 2H), 7.47(dd, 1H, J=8.8 Hz, 2.4 Hz), 7.60 (m, 1H), 7.65-7.68 (m, 4H), 7.85 (d, 1H, J=8Hz), 8.00 (td, 1H, J=7.6 Hz, 2 Hz), 8.71 (bd, 1H, J=4.8 Hz). MS: m/z 429.9 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0616ff4fe09d49cbaea1000a951d0f30
출처 메모uspto-grants-2008_09