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3-Fluorobenzenesulfonamide → 5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-fluorophenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Fluorobenzenesulfonamide | HCID 150924 | — |
| 反応物 | 4-[(1S)-1-({[5-Chloro-2-(4-fluorophenoxy)pyridin-3-YL]carbonyl}amino)ethyl]benzoic acid | HCID 11683088 | — |
| 生成物 | 5-Chloro-2-(4-fluorophenoxy)-N-{(1S)-1-[4-({[(3-fluorophenyl)sulfonyl]amino}carbonyl)phenyl]ethyl}nicotinamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07238714B2 |
| 出典データセット | uspto-grants-2007_07 |
| ORD ID | ord-5f427bcfdb984dd6ac710e037a0090e0 |
| 出典メモ | uspto-grants-2007_07 |