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HRID 228625作成日:2026年10月26日

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

https://huagongshe.com/reaction/228625

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-hydroxy-6-methylbenzoateHCID 584222—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物Ethyl 2-[(6,7-dimethoxy-4-quinolyl)oxy]-6-methylbenzoateHCID 5775635091.3%

反応条件

温度120 °C

反応手順

4-Chloro-6,7-dimethoxyquinoline (112 mg), ethyl 6-methylsalicylate (360 mg), and 4-dimethylaminopyridine (244 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight and was further stirred at 140° C. for 2 hr. 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 residue, 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, and the residue was purified by column chromatography using acetone-hexane to give the title compound (168 mg, yield 91%).

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-9845176dbbe1460683bc8cdfa08873e6
出典メモuspto-grants-2009_07