戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 384445作成日:2026年10月26日

Potassium Carbonate → ethyl 3-{[4-(benzyloxy)-3-methylquinolin-2-yl]methoxy}-5-(tetrahydro-2H-pyran-4-ylmethoxy)benzoate

https://huagongshe.com/reaction/384445

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-(Bromomethyl)oxaneHCID 2773286—
反応物Ethyl 3-{[4-(benzyloxy)-3-methylquinolin-2-yl]methoxy}-5-hydroxybenzoateHCID 59527065—
溶媒DimethylformamideHCID 6228—
生成物ethyl 3-{[4-(benzyloxy)-3-methylquinolin-2-yl]methoxy}-5-(tetrahydro-2H-pyran-4-ylmethoxy)benzoateHCID 5952740197.5%

反応条件

温度80 °C

反応手順

A mixture of ethyl 3-{[4-(benzyloxy)-3-methylquinolin-2-yl]methoxy}-5-hydroxybenzoate (2.10 g), 4-(bromomethyl)tetrahydro-2H-pyrane (2.29 g), potassium carbonate (0.98 g), and DMF (40 mL) was stirred at 80° C. for 13 hours. The reaction mixture was concentrated under reduced pressure, and then water was added to the residue, followed by extraction with ethyl acetate (150 mL). The organic layer was washed sequentially with water and saturated brine, and dried. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol=20/1) to obtain ethyl 3-{[4-(benzyloxy)-3-methylquinolin-2-yl]methoxy}-5-(tetrahydro-2H-pyran-4-ylmethoxy)benzoate (2.50 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367702B2
出典データセットuspto-grants-2013_02
ORD IDord-2e07592495294ee89e1737827a91f1e2
出典メモuspto-grants-2013_02