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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

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methyl-3-phenylisoxazole-4-carbonyl chlorideHCID 85624—
反応物4-Amino-7-(trifluoromethyl)quinolineHCID 2735960—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物5-methyl-3-phenyl-N-(7-trifluoromethyl-4-quinolinyl)-4-isoxazolecarboxamideHCID 6000792055.8%

反応条件

温度70 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008501B2
出典データセットuspto-grants-2011_08
ORD IDord-6295f13d93eb4c04991ec4eacba7f6e4
出典メモuspto-grants-2011_08