戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 634362作成日:2026年10月26日

Cesium carbonate → 3-(1-Hydroxyethyl)-4-(4-(2-morpholinoethoxy)phenyl)-1H-isochromen-1-one

https://huagongshe.com/reaction/634362

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-(2-Morpholin-4-ylethoxy)benzeneboronic acid, pinacol esterHCID 4625910—
反応物4-Bromo-3-(1-hydroxyethyl)-1H-isochromen-1-oneHCID 118131255—
触媒HCID 178418397HCID 178418397—
生成物3-(1-Hydroxyethyl)-4-(4-(2-morpholinoethoxy)phenyl)-1H-isochromen-1-oneHCID 11813130133.5%

反応手順

The title compound was made in a similar way as that of the intermediate B1, using 4-bromo-3-(1-hydroxyethyl)-1H-isochromen-1-one (Intermediate A2, 0.36 g, 1.35 mmol), 4-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)-morpholine (0.45 g, 1.35 mmol), Pd(PPh3)4 (0.078 g, 0.068 mmol) and Cs2CO3 (0.53 g, 1.6 mmol). The crude was filtered, diluted with 1M HClaqueous (3 ml) and purified via reverse phase chromatography with a Biotage C18 SNAP 120 g column (Phase A, water 95%, ACN 4.9%, formic acid 0.1%); Phase B ACN 99.9%, formic acid 0.1%) to afford the title compound (0.179 g, 33%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321776B2
出典データセットuspto-grants-2016_04
ORD IDord-afa818dd489e4ba094a373f5f0c4aa08
出典メモuspto-grants-2016_04