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HRID 239696作成日:2026年10月24日

Dichloromethane → 4-(4-amino-1-(1-(3-(3-fluorophenyl)-4-oxo-4H-chromen-2-yl)ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl)thiophene-2-carbaldehyde

https://huagongshe.com/ja/reaction/239696

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium CarbonateHCID 10340—
反応物2-Formylthiophene-4-boronic acidHCID 11084115—
反応物2-(1-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-3-(3-fluorophenyl)-4H-chromen-4-oneHCID 66579932—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-(4-amino-1-(1-(3-(3-fluorophenyl)-4-oxo-4H-chromen-2-yl)ethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl)thiophene-2-carbaldehydeHCID 8707159319.2%

反応条件

温度80 °C

反応手順

To a solution of Example 57c (0.350 g, 0.663 mmoles) in DMF (5 ml), ethanol (2.5 ml) and water (2.5 ml), 2-formyl-4-thiopheneboronic acid (0.155 g, 0.995 mmoles) and sodium carbonate (0.210 g, 1.98 mmoles) were added and the system is degassed for 30 min. Tetrakistriphenylphosphine Palladium (0.038 g, 0.033 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 light brown solid (0.065 g, 19% yield). MP: 192-195° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 10.01(s,1H), 8.30(s,1H), 8.24(s,1H), 8.07(s,1H), 8.05(dd, J=7.9,1.4 Hz, 1H), 7.85(m,1H),7.69(d, J=8.4 Hz, 1H),7.53(t, J=7.8 Hz, 1H),7.28(br s,1H), 7.06(t, J=8.8 Hz, 1H),6.93(br s, 2H), 6.04(q, J=7.0 Hz, 1H),1.89(d, J=7.0 Hz, 3H). Mass: 511.95(M+).

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-5a84b93fd4284f0e9ed6f0d8d4c736ec
出典メモuspto-grants-2014_02