反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
4,6-dichloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-d]pyrimidine (100 mg, 0.366 mmol), (3-acrylamidophenyl)boronic acid (70 mg, 0.366 mmol) and triphenylphosphine (4 mg, 0.015 mmol) were dissolved in a mixture of toluene (7 mL) and 1 M sodium carbonate (39 mg, 0.367 mmol). Palladium(II) acetate (2.0 mg, 0.009 mmol) was then added and the reaction mixture was stirred for 12 h at 80° C. The reaction mixture was then allowed to cool to room temperature and the solvent was removed in vacuo. The residue was dissolved in EtOAc (20 mL) and washed with water (10 mL). The organic layer was separated, the aqueous layer was extracted with EtOAc (20 ml), and organic layers were combined. The combined organic layers were washed with brine (20 mL), dried over Na2SO4 and then concentrated. The crude material was purified by flash chromatography (EtOAc/hexane 20%) to yield the title compound (70%). 1H NMR (400 MHz, CDCl3): δ 8.45 (m, 2H), 7.88 (d, 1H, J=8.0 Hz), 7.85 (d, 1H, J=8.0 Hz), 7.68 (s, 1H), 7.49 (t, 1H, J=8.0 Hz), 6.46 (m, 1H), 6.27 (m, 1H), 6.06 (d, 1H, J=10.4 Hz), 5.79 (d, 1H, J=10.0 Hz), 4.12 (m, 1H), 3.82 (t, 1H, J=10.0 Hz), 2.58 (m, 1H), 2.14 (m, 1H), 1.95 (m, 1H), 1.78 (m, 2H), 1.62 (m, 1H). ESI-MS: 384.10 [M+H]+.
WORKUP
后处理
- temperatureto cool to room temperature
- customthe solvent was removed in vacuo
- dissolutionThe residue was dissolved in EtOAc (20 mL)
- washwashed with water (10 mL)
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with EtOAc (20 ml), and organic layers
- washThe combined organic layers were washed with brine (20 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe crude material was purified by flash chromatography (EtOAc/hexane 20%)