Réaction #161

ord-203f818b7f344d11a82d6bc3539ff565

Équation de réaction

Clc1ccnc(Cl)c1
Clc1ccnc(Cl)c1
Nc1ccccc1
Nc1ccccc1
Clc1ccnc(Nc2ccccc2)c1
Clc1ccnc(Nc2ccccc2)c
Rendement 55.8%

Solvants

Conditions de réaction

Température
100°CELSIUS

Mode opératoire

diacetoxypalladium (0.303 g, 1.35 mmol) was added in one portion to a degassed mixture of 2,4-dichloropyridine (10 g, 67.57 mmol), aniline (6.29 g, 67.57 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (1.173 g, 2.03 mmol) and cesium carbonate (44.0 g, 135.14 mmol) in dioxane (250 mL) under argon. The resulting mixture was stirred at 100 °C for 24 hours. The mixture was then cooled to room temperature, filtered and concentrated to dryness to give the crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford 4-chloro-N-phenylpyridin-2-amine (7.72 g, 55.8 %) as a pale orange solid.

Source

750 AstraZeneca ELN dataset