反应详情

温度

80 °C

A microwave vial was charged with 6-(cis-2-amino-3,3-difluorocyclohexylamino)-4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (13.7 mg, 0.028 mmol) and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (8.82 mg, 0.042 mmol) and bis(triphenylphosphine)palladium chloride (3.97 mg, 5.65 μmol) and placed under an inert environment. DME (283 μL) was added to the mixture and the resulting yellow slurry was degassed for 5 min. Sodium carbonate was added (56.5 μL, 0.113 mmol) and the slurry degassed for an additional 3 min. The vessel was capped and the mixture was heated at 80° C. for 4 h, cooled to ambient temperature, diluted with EtOAc (5 mL), and washed with water (3 mL) and brine (3 mL). The organic layer was collected, dried over sodium sulfate, and concentrated to give the title compound as a dark brown residue which was used in the next step without further purification (21 mg). [M+H] calc'd for C26H29F3N6O3, 531. found, 531.

1. customthe resulting yellow slurry was degassed for 5 min
2. additionSodium carbonate was added (56.5 μL, 0.113 mmol)
3. customthe slurry degassed for an additional 3 min
4. customThe vessel was capped
5. temperaturecooled to ambient temperature
6. additiondiluted with EtOAc (5 mL)
7. washwashed with water (3 mL) and brine (3 mL)
8. customThe organic layer was collected
9. dry with materialdried over sodium sulfate
10. concentrationconcentrated