Reacción #164

ord-d638b772d95f46ee990c617a7a9864d8

Ecuación de reacción

FC(F)(F)c1cnc(Cl)cc1I
FC(F)(F)c1cnc(Cl)cc1
CNC(=O)c1ccccc1N
CNC(=O)c1ccccc1N
CNC(=O)c1ccccc1Nc1cc(Cl)ncc1C(F)(F)F
CNC(=O)c1ccccc1Nc1cc
Rendimiento 67.4%

Disolventes

Condiciones de reacción

Temperatura
90°CELSIUS

Procedimiento

2-chloro-4-iodo-5-(trifluoromethyl)pyridine (7 g, 22.77 mmol), 2-amino-N- methylbenzamide (3.42 g, 22.77 mmol), diacetoxypalladium (0.409 g, 1.82 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (2.108 g, 3.64 mmol) and cesium carbonate (8.90 g, 27.32 mmol) were mixed together in dioxane (140 mL). Reaction was degassed with nitrogen and was stirred at 90 °C overnight under nitrogen. Reaction was filtered, washed with CH2Cl2 and filtrate was concentrated to dryness. The crude product was purified by flash chromatography on silica gel eluting with 10 to 50% ethyl acetate in petroleum ether. The solvent was evaporated to dryness to afford 2-(2-chloro-5-(trifluoromethyl)pyridin-4-ylamino)-N-methylbenzamide (5.06 g, 67.4 %) as a pale yellow solid.

Fuente

750 AstraZeneca ELN dataset