Reacción #746

ord-effcbe0533904d0880f0ace9776ccb21

Ecuación de reacción

CNC(=O)c1cc(Cl)nc(Cl)c1
CNC(=O)c1cc(Cl)nc(Cl
Nc1ccccc1
Nc1ccccc1
CNC(=O)c1cc(Cl)nc(Nc2ccccc2)c1
CNC(=O)c1cc(Cl)nc(Nc
Rendimiento 52.9%

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS

Procedimiento

SODIUM TERT-BUTOXIDE (0.984 g, 10.24 mmol) was added to 2,6-dichloro-N- methylisonicotinamide (1.5 g, 7.32 mmol), ANILINE (0.667 mL, 7.32 mmol), PALLADIUM(II) ACETATE (0.016 g, 0.07 mmol) and XANTPHOS (0.127 g, 0.22 mmol) in toluene (30 mL) under nitrogen. The resulting mixture was stirred at 80 °C for 4 hours. The reaction mixture was evaporated to dryness and redissolved in EtOAc (100 mL), and washed sequentially with water (2 x 50 mL) and saturated brine (50 mL). The organic layer was dried over MgSO4, filtered and preadsorbed onto silica. The crude product was purified by flash silica chromatography, elution gradient 30 to 80% EtOAc in heptane. Pure fractions were evaporated to dryness to afford 2-chloro-N- methyl-6-(phenylamino)isonicotinamide (1.012 g, 52.9 %) as a cream solid.

Fuente

750 AstraZeneca ELN dataset