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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1293277생성일: 2026년 10월 26일

4-[(1S)-1-({[5-Chloro-2-(4-fluorophenoxy)pyridin-3-YL]carbonyl}amino)ethyl]benzoic acid → 5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-methoxyphenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamide

https://huagongshe.com/reaction/1293277

반응식

참여 물질

역할이름HCID투입량
반응물4-[(1S)-1-({[5-Chloro-2-(4-fluorophenoxy)pyridin-3-YL]carbonyl}amino)ethyl]benzoic acidHCID 11683088—
반응물3-Methoxybenzene-1-sulfonamideHCID 14763060—
생성물5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-methoxyphenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamideHCID 58905321—

반응 단계

The title compound was prepared according to the procedure described in step 1 of Example 103 from 4-[(1S)-1-({[5-chloro-2-(4-fluorophenoxy)pyridin-3-yl]carbonyl}amino)ethyl]benzoic acid (step 5 of Example 44) and 3-methoxybenzenesulfonamide: 1H-NMR (CDCl3) δ 8.51 (1H, d, J=2.8 Hz), 8.13 (1H, d, J=2.8 Hz), 8.09 (1H, d, J=7.0 Hz), 7.73 (2H, d, J=8.4 Hz), 7.70–7.64 (2H, m), 7.49–7.39 (3H, m), 7.21–7.08 (5H, m), 5.37–5.25 (1H, m), 3.88 (3H, s), 1.56 (3H, d, J=6.8 Hz); MS (ESI) m/z 584 (M+H)+, 582 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07238714B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-f48ad34f3650480ab3e48b198cf40ce1
출처 메모uspto-grants-2007_07