Reacción #651
ord-15613520ef9b4d099659a0a3ac545228
Ecuación de reacción
Brc1ccncc1
OC1CCNC1
→
OC1CCN(c2ccncc2)C1
Rendimiento 43.0%
Reactantes
Disolventes
Condiciones de reacción
Temperatura
65°CELSIUS
Procedimiento
In a 50 ml round bottomed flask THF (1 mL) was added to a mixture of 4-bromopyridine (1 g, 6.33 mmol), pyrrolidin-3-ol (0.662 g, 7.60 mmol),2-(dimethylamino)-2'-(dicyclohexylphosphino)biphenyl (0.249 g, 0.63 mmol) and Pd2(dba)3 (0.580 g, 0.63 mmol). To the slurry lithium bis(trimethylsilyl)amide (13.92 mL, 13.92 mmol) was added dropwise at 0 °C and the solution was refluxed at 65 °C overnight for 20 hrs. The reaction mixture was passed through celite, concentrated and column purified (0-20%MeOH/DCM) to obtain 0.447 mg of product.
Fuente
750 AstraZeneca ELN dataset