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HRID 229042作成日:2026年10月24日

Water → 3-(6,7-Dimethoxy-quinolin-4-yloxy)-naphthalen-2-ol

https://huagongshe.com/ja/reaction/229042

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,3-DihydroxynaphthaleneHCID 7091—
反応物4-Chloro-6,7-dimethoxyquinolineHCID 459610—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物3-(6,7-Dimethoxy-quinolin-4-yloxy)-naphthalen-2-olHCID 2307832758.4%

反応条件

温度130 °C

反応手順

Naphthalene-2,3-diol (1.00 g), 4-chloro-6,7-dimethoxyquinoline (691 mg), and 4-dimethylaminopyridine (1.14 g) were suspended in o-dichlorobenzene (20 ml), and the mixture was stirred at 130° C. for one hr. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was then washed with water and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform-methanol to give the title compound (627 mg, yield 58%).

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-14bf1f949cbb41b0bca79364bb9d621e
出典メモuspto-grants-2009_07