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HRID 228591作成日:2026年10月26日

2-Hydroxy-5-methylbenzophenone → {2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}-(phenyl)methanone

https://huagongshe.com/reaction/228591

反応式

関与物質

役割名称HCID仕込み量
反応物2-Hydroxy-5-methylbenzophenoneHCID 73851—
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}-(phenyl)methanoneHCID 2487906195%

反応条件

温度160 °C

反応手順

4-Chloro-6,7-dimethoxyquinoline (58.6 mg), 2-hydroxy-5-methylbenzophenone (276 mg), and 4-dimethylaminopyridine (156 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 5 hr. The reaction solution was cooled to room temperature, and the solvent was then removed therefrom by distillation under the reduced pressure. Chloroform was added to the residue, and the mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform and by thin layer chromatography using acetone-hexane to give the title compound (98.9 mg, yield 95%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560558B2
出典データセットuspto-grants-2009_07
ORD IDord-e30471ad9dc540d0ab6ae9ecab3322aa
出典メモuspto-grants-2009_07