反应 #45551

反应方程式

N-(3-Bromo-6-cyano-4-iodo-2-methoxy-5-methylphenyl)-2,2-dimethylpropionamide

3-benzyloxybenzeneboronic acid

tripotassium phosphate

→

compound

收率 55.0%

N-(3′-Benzyloxy-2-bromo-5-cyano-3-methoxy-6-methylbiphenyl-4-yl)-2,2-dimethylpropionamide

收率 55.0%

溶剂

ethyl acetate

反应条件

后处理

1. 1
   其他by purging with nitrogen
2. 2
   其他N,N-Dimethylformamide (20 ml) was injected into it with a syringe
3. 3
   温度After cooling
4. 4
   其他the reaction liquid
5. 5
   洗涤successively washed with saturated brine (×3), 1 N hydrochloric acid, saturated brine
6. 6
   干燥an aqueous saturated sodium hydrogencarbonate solution and saturated brine, dried on anhydrous magnesium sulfate
7. 7
   浓缩the solvent was concentrated under reduced pressure
8. 8
   其他to obtain a pale brown residue
9. 9
   其他The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1)

实验过程

N-(3-Bromo-6-cyano-4-iodo-2-methoxy-5-methylphenyl)-2,2-dimethylpropionamide (I-6) (1.02 g, 2.26 mmol), 3-benzyloxybenzeneboronic acid (541 mg, 2.37 mmol), tripotassium phosphate (74-85%, 1.30 g, 4.52 mmol) and tetrakis(triphenylphosphine)palladium(0) (261 mg, 0.226 mmol) were added to a 50-ml eggplant-type flask, followed by purging with nitrogen. N,N-Dimethylformamide (20 ml) was injected into it with a syringe, followed by stirring at 95° C. for 4 hours. After cooling, the reaction liquid was diluted with ethyl acetate, successively washed with saturated brine (×3), 1 N hydrochloric acid, saturated brine, an aqueous saturated sodium hydrogencarbonate solution and saturated brine, dried on anhydrous magnesium sulfate, then the solvent was concentrated under reduced pressure to obtain a pale brown residue. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1) to obtain the entitled compound (630 mg, 55%) as a pale brown solid.

来源