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HRID 228944作成日:2026年10月25日

Water → 3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6-dimethyl-[2,3']bipyridine

https://huagongshe.com/reaction/228944

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
反応物5,6-Dimethyl-3-hydroxy-[2,3']bipyridineHCID 23156516—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6-dimethyl-[2,3']bipyridineHCID 5775657188%

反応条件

温度140 °C

反応手順

5,6-Dimethyl-3-hydroxy-[2,3′]bipyridine (400 mg), 7-benzyloxy-4-chloro-6-methoxyquinoline (1.80 g), and 4-dimethylaminopyridine (732 mg) were suspended in o-dichlorobenzene (8 ml), and the suspension was stirred at 140° C. for 6 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 washed with saturated brine and was dried over anhydrous sodium 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 (811 mg, yield 88%).

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-3e25a30de33343f69056d7bdd3a84c10
出典メモuspto-grants-2009_07