反应详情

In a quartz vial, (5-chloro-1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-[5-(4-fluoro-benzylamino)-2-(4-methoxy-benzyl)-2H-pyrazol-3-yl]-methanol (148, 0.328 g, 0.506 mmol) was combined with 20 mL of dichloromethane, triethylsilane (0.4 mL, 2.0 mmol) was added, followed by trifluoroacetic acid (0.2 mL, 2.0 mmol). The reaction was stirred overnight at room temperature, then concentrated under vacuum and ethyl acetate was added. This was washed with 1 M aqueous potassium carbonate and brine, dried with sodium sulfate, and purified by silica gel column chromatography, eluting with 2-20% methanol in dichloromethane. Appropriate fractions were combined and concentrated under vacuum, and the solid further washed with ethyl acetate and hexane to provide the desired compound. 1H NMR was consistent with compound structure.

1. additionwas added
2. concentrationconcentrated under vacuum and ethyl acetate
3. additionwas added
4. washThis was washed with 1 M aqueous potassium carbonate and brine
5. dry with materialdried with sodium sulfate
6. custompurified by silica gel column chromatography
7. washeluting with 2-20% methanol in dichloromethane
8. concentrationconcentrated under vacuum
9. washthe solid further washed with ethyl acetate and hexane