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HRID 70813作成日:2026年10月24日

Trifluoroacetic anhydride → 2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxide

https://huagongshe.com/ja/reaction/70813

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物Carbamide PeroxideHCID 31294—
反応物2-Cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamideHCID 86672971—
溶媒DichloromethaneHCID 6344—
生成物2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxideHCID 8667297081%

反応手順

2-Cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide (240 mg) was dissolved in dichloromethane, added with urea-hydrogen peroxide adduct (85 mg) and trifluoroacetic anhydride (190 mg), and stirred at room temperature for 20 hours. The reaction solution was concentrated under the reduced pressure, and the resulting residues were dissolved in ethyl acetate. The solution was washed with water and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the solvent was removed by distillation under the reduced pressure. The resulting residues were purified by column chromatography to obtain 2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxide (0.20 g, 81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822691B2
出典データセットuspto-grants-2014_09
ORD IDord-df3e9f22808e44b8a724cb76231ba676
出典メモuspto-grants-2014_09