反应详情

温度

85 °C

To [4-(3-chloro-phenyl)-2-methoxy-quinolin-6-yl]-(6-methyl-pyridin-3-yl)-(3-methyl-3H-imidazol-4-yl)-methanol (0.118 g, 0.251 mmol) in toluene (5 ml) under an atmosphere of dry N2 was added thionyl chloride (0.18 ml, 2.51 mmol) dropwise. The reaction mixture was heated at 85° C. for 15 hours. Solvent and the excess thionyl chloride were removed under reduced pressure. The crude chloride was taken up in toluene and concentrated under vacuum. The resulting solid was dissolved in THF (10 mL) and to this solution at −78° C. was bubbled ammonia gas (NH3) for 10 minutes. The reaction mixture was stirred at ambient temperature under an atmosphere of N2 for additional 1.5 hours. After removal of THF, the product mixture was partitioned between CHCl3 and water. The organic layer was washed, dried over MgSO4 and concentrated under vacuum to give a brown solid. This was chromatographed on silica gel with CHCl3 then MeOH—CHCl3—NH4OH (5:95:0.1 to 10:89:1) as eluents to afford the title compound of Example 14A as a white solid (53 mg, 0.116 mmol, 46.4% yield).

1. customSolvent and the excess thionyl chloride were removed under reduced pressure
2. concentrationconcentrated under vacuum
3. dissolutionThe resulting solid was dissolved in THF (10 mL) and to this solution at −78° C.
4. customwas bubbled ammonia gas (NH3) for 10 minutes
5. customAfter removal of THF
6. customthe product mixture was partitioned between CHCl3 and water
7. washThe organic layer was washed
8. dry with materialdried over MgSO4
9. concentrationconcentrated under vacuum
10. customto give a brown solid
11. customThis was chromatographed on silica gel with CHCl3