反应详情

Dissolve 1-{2-[4-(6-benzyloxy-2-bromo-benzo[b]thiophen-3-yloxy)-phenoxy]-ethyl}-piperidine (350 mg, 0.65 mmol) and 3-fluoro-4-methanesulfonyl-phenyl-boronic acid (213 mg, 0.98 mmol) in dioxane (10 mL) and add 10% aqueous sodium carbonate (9 mL) and Pd(PPh3)4 (75 mg, 0.065 mmol). Heat to reflux for 3 hours. Partition the reaction mixture between dichloromethane (20 mL) and saturated aqueous ammonium chloride (20 mL). Wash the organic layer with brine (30 mL), dry with sodium sulfate, and concentrate in vacuo. Chromatograph the residue on a SiO2 column eluting with methanol in dichloromethane (0 to 5%) to give 150 mg of the title compound contaminated with a 2-H reduced byproduct. Take the mixture on to the next step without further purification.

1. temperatureHeat
2. temperatureto reflux for 3 hours
3. customPartition the reaction mixture between dichloromethane (20 mL) and saturated aqueous ammonium chloride (20 mL)
4. washWash the organic layer with brine (30 mL)
5. dry with materialdry with sodium sulfate
6. concentrationconcentrate in vacuo
7. washChromatograph the residue on a SiO2 column eluting with methanol in dichloromethane (0 to 5%)