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HRID 228590作成日:2026年10月25日

5-Bromo-2-hydroxybenzophenone → {5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanone

https://huagongshe.com/reaction/228590

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-hydroxybenzophenoneHCID 229009—
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物{5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanoneHCID 2487921094.5%

反応条件

温度160 °C

反応手順

4-Chloro-6,7-dimethoxyquinoline (56.1 mg), 5-bromo-2-hydroxybenzophenone (361 mg), and 4-dimethylaminopyridine (168 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 7 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 mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous magnesium 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 (110 mg, yield 94%).

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-6f3beb0d05994b94832df27083e012ea
出典メモuspto-grants-2009_07