Reacción #657325

ord-69c649098ac94325996a832ab2d007a6

Ecuación de reacción

Brc1c(-c2ccccc2)nn2cccnc12
3-Bromo-2-phenylpyrazolo[1,5-a]pyrimidine
CC(C)(C)OC(=O)Nc1cc(B2OC(C)(C)C(C)(C)O2)ccn1
tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate
CC(C)(C)OC(=O)Nc1cc(B2OC(C)(C)C(C)(C)O2)ccn1
Tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Nc1cc(-c2c(-c3ccccc3)nn3cccnc23)ccn1
4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine
Rendimiento 45.8%

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture is flushed with argon for 5 mins
  2. 2
    Otrosealed
  3. 3
    Temperaturathe mixture is heated for 2 h at 120° C
  4. 4
    Extracciónextracted with ethyl acetate (3×50 mL)
  5. 5
    SecadoThe organic layer is dried over anhydrous magnesium sulphate
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated under reduced pressure
  8. 8
    OtroThe crude material is purified by column chromatography

Procedimiento

3-Bromo-2-phenylpyrazolo[1,5-a]pyrimidine (1.0 g, 3.65 mmol) and tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate (1.29 g, 4.01 mmol, 1.1 eq) are dissolved in 10 mL 1,4-dioxan. To this mixture bis(tricyclohexylphosphine)palladium(II)-dichloride (269 mg, 0.37 mmol, 0.1 eq) and 9.1 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 90 min at 120° C. in the microwave (Biotage). Tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate (214 mg, 1.4 mmol, 0.37 eq) and bis(tricyclohexylphosphine)palladium(II)-dichloride (269 mg, 0.37 mmol, 0.1 eq) are then added and the mixture is heated for 2 h at 120° C. The reaction mixture is then poured in water and extracted with ethyl acetate (3×50 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in heptane and ethyl acetate (1:0 to 1:1) as eluent and 0.48 g (44%) of 4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine are obtained as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09023844B2uspto-grants-2015_05