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HRID 239636作成日:2026年10月27日

Sodium Carbonate → 3-(2,3-dihydrobenzofuran-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/239636

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物(2,3-Dihydro-1-benzofuran-5-yl)boronic acidHCID 2773380—
反応物HCID 178508725HCID 178508725—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(2,3-dihydrobenzofuran-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 178508703—

反応条件

温度80 °C

反応手順

To a solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.70 g, 2.68 mmoles) in DMF (10 ml), ethanol (6 ml) and water (6 ml), 2,3-dihydrobenzofuran-5-boronic acid (0.527 g, 3.21 mmoles) and sodium carbonate (0.852 g, 8.04 mmoles) were added and the system is degassed for 30 min. Tetrakistriphenylphosphine Palladium (0.610 g, 0.528 mmoles) was added under nitrogen atmosphere and heated to 80° C. After 12 h, the reaction mixture was celite filtered, concentrated and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as brown solid (0.198 g, 29% yield1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 13.42(s,1H), 8.18(s,1H), 7.48(s,1H), 7.36(d, J=8.1 Hz, 1H), 6.90(d, J=8.2 Hz, 1H), 4.61(d, J=8.7 Hz, 2H),3.27(d, J=8.7 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642607B2
出典データセットuspto-grants-2014_02
ORD IDord-055b622c187c4cc18ec3cdbaa6446188
出典メモuspto-grants-2014_02