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
- 105 °C
PROCEDURE
实验过程
1.03 g of 2-[5-cyclopropyl-1-(4-methoxybenzyl)-4-methyl-1H-pyrazol-3-yl]-5-methoxypyrimidin-4-amine (2.82 mmol, 1.00 eq.), 603 mg of 4-bromopyridine hydrochloride (1:1) (3.10 mmol, 1.10 eq.), 245 mg of (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.423 mmol, 0.15 eq.), 2.76 g of cesium carbonate (8.46 mmol, 3.00 eq.) and 63 mg of palladium diacetate (0.282 mmol, 0.1 eq.) were suspended in 10.8 mL of dry DMF and stirred under nitrogen atmosphere at 105° C. bath temperature for two hours. The reaction mixture was diluted with water and the crude product was extracted with DCM. The combined organic layers were dried over a silicon filter and concentrated in vacuo. The residue was purified by flash chromatography yielding 930 mg (1.95 mmol, 69%) of analytically pure target compound.
WORKUP
后处理
- extractionthe crude product was extracted with DCM
- customThe combined organic layers were dried over a silicon
- filtrationfilter
- concentrationconcentrated in vacuo
- customThe residue was purified by flash chromatography
- customyielding 930 mg (1.95 mmol, 69%) of analytically pure target compound