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HRID 228620作成日:2026年10月26日

4-Chloro-6,7-dimethoxyquinoline → Ethyl 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-(2,4-difluorophenyl)benzoate

https://huagongshe.com/reaction/228620

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
反応物Ethyl 2',4'-Difluoro-4-hydroxy[1,1'-biphenyl]-3-carboxylateHCID 23078331—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物Ethyl 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-(2,4-difluorophenyl)benzoateHCID 5775644824%

反応条件

温度120 °C

反応手順

Ethyl 5-(2,4-difluorophenyl)salicylate (188 mg), 4-chloro-6,7-dimethoxyquinoline (57 mg), and 4-dimethylaminopyridine (93 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure. The residue was purified by column chromatography using acetone-hexane to give the title compound (13 mg, yield 24%).

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-5b1485f1413d4bbda7b3af624a1e565c
出典メモuspto-grants-2009_07