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HRID 1293275作成日:2026年10月27日

3-Fluorobenzenesulfonamide → 5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-fluorophenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamide

https://huagongshe.com/reaction/1293275

反応式

関与物質

役割名称HCID仕込み量
反応物3-FluorobenzenesulfonamideHCID 150924—
反応物4-[(1S)-1-({[5-Chloro-2-(4-fluorophenoxy)pyridin-3-YL]carbonyl}amino)ethyl]benzoic acidHCID 11683088—
生成物5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-fluorophenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamideHCID 58905369—

反応手順

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-fluorobenzenesulfonamide: 1H-NMR (CDCl3) δ 8.86 (1H, br.s), 8.51 (1H, d, J=2.6 Hz), 8.13 (1H, d, J=2.6 Hz), 8.14–8.08 (1H, m), 7.98–7.91 (1H, m), 7.89–7.81 (1H, m), 7.73 (2H, d, J=8.3 Hz), 7.61–7.50 (1H, m), 7.42 (2H, d, J=8.3 Hz), 7.40–7.30 (1H, m), 7.21–7.08 (4H, m), 5.37–5.24 (1H, m), 1.57 (3H, d, J=6.8 Hz); MS (ESI) m/z 572 (M+H)+, 570 (M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07238714B2
出典データセットuspto-grants-2007_07
ORD IDord-5f427bcfdb984dd6ac710e037a0090e0
出典メモuspto-grants-2007_07