Reacción #657316

Ecuación de reacción

sodium carbonate

3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine

tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate

→

4-(2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl)pyridin-2-amine

Disolventes

1,4-dioxan

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe reaction mixture is flushed with argon for 5 mins
2. 2
   Otrosealed
3. 3
   Otroall crude reaction mixtures
4. 4
   TemperaturaAfter cooling
5. 5
   Filtracióninsoluble components are filtered off over Celite
6. 6
   Lavadothe residue washed with 1,4-dioxan
7. 7
   OtroThe organic phase is evaporated
8. 8
   Otrothe crude product purified by column chromatography over silica gel
9. 9
   OtroAfter evaporation of the solvents 2.10 g (41%) of 4-(2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl)pyridin-2-amine
10. 10
    Otroare obtained as a colourless solid

Procedimiento

3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (700 mg, 2.25 mmol) and tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate (792 mg, 2.47 mmol, 1.1 eq) are dissolved in 10 mL 1,4-dioxan. To this mixture Bis(tricyclohexylphosphine)palladium(II)-dichloride (166 mg, 0.22 mmol, 0.1 eq) and 5.4 mL sodium carbonate solution (2 molar) are added. The reaction mixture is flushed with argon for 5 mins and then sealed. Next the mixture is heated for 12 mins at 150° C. in the microwave (Biotage). The procedure is repeated 7× using the same scale and all crude reaction mixtures are combined thereafter. After cooling, insoluble components are filtered off over Celite and the residue washed with 1,4-dioxan. The organic phase is evaporated and the crude product purified by column chromatography over silica gel using dichloromethane/methanole as eluent. After evaporation of the solvents 2.10 g (41%) of 4-(2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl)pyridin-2-amine are obtained as a colourless solid.

Fuente