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HRID 49122作成日:2026年10月23日

Ethanol → 6-Pyridin-3-yl-1,3-dihydro-indol-2-one

https://huagongshe.com/ja/reaction/49122

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
反応物Pyridine-3-boronic acid propane diolHCID 69587225—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物6-Pyridin-3-yl-1,3-dihydro-indol-2-oneHCID 2191557942%

反応条件

温度100 °C

反応手順

To a solution of 6-bromo-2-oxindole (4 g, 26.3 mmol) dissolved in 60 mL of toluene and 60 mL of ethanol with stirring and a little heating tetrakis(triphenyl-phosphine)palladium(0) (2.3 g, 1.9 mmol) was added followed by a 2M aqueous solution of sodium carbonate (50 mL, 100 mmol) and pyridine-3-boronic acid propane diol (5 g, 30.7 mmol). The mixture was heated in a 100° C. oil bath for 12 hours. The cooled reaction was diluted with ethyl acetate (500 mL), washed with saturated aqueous sodium bicarbonate (200 mL), water (200 mL) and brine (200 mL). The organic layer was dried with magnesium sulfate and concentrated to afford a brown solid. The residue was triturated with methylene chloride/diethyl ether to give 2.32 g (42%) of 6-pyridin-3-yl-1,3-dihydro-indol-2-one as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706709B2
出典データセットuspto-grants-2004_03
ORD IDord-c51a563b1d5e48e99b901ce71d587a2a
出典メモuspto-grants-2004_03