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HRID 1678309作成日:2026年10月27日
5-Methyl-3-phenylisoxazole-4-carbonyl chloride → 5-methyl-3-phenyl-N-(7-trifluoromethyl-4-quinolinyl)-4-isoxazolecarboxamide
https://huagongshe.com/reaction/1678309
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 5-Methyl-3-phenylisoxazole-4-carbonyl chloride | HCID 85624 | — |
| 反応物 | 4-Amino-7-(trifluoromethyl)quinoline | HCID 2735960 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-methyl-3-phenyl-N-(7-trifluoromethyl-4-quinolinyl)-4-isoxazolecarboxamide | HCID 60007920 | 55.8% |
反応手順
5-Methyl-3-phenylisoxazole-4-carbonyl chloride (100 mg) and 4-amino-7-trifluoromethylquinoline (250 mg) were dissolved in dichlorormethane (5 mL) and pyridine (0.3 mL). The reaction solution was heated at 70° C. overnight and then diluted with ethyl acetate (60 mL). The organic solution was washed with water (60 mL), dried, evaporated and purified by flash column chromatography (EtOAc/hexanes=1/6) to give 5-methyl-3-phenyl-N-(7-trifluoromethyl-4-quinolinyl)-4-isoxazolecarboxamide (100 mg) as a white solid. 1H NMR (CDCl3): δ 2.91 (s, 3H), 7.33-7.69 (m, 9H), 8.39 (s, 1H, NH), 8.99 (d, J=5.1 Hz, 1H); 19F NMR (282 MHz, CDCl3): δ-63.26; LCMS: ret. time: 34.04 min.; purity: 98.90%; MS (m/e): 398.77 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08008501B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-6295f13d93eb4c04991ec4eacba7f6e4 |
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| 出典メモ | uspto-grants-2011_08 |
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