Reacción #162062

ord-147cd01489ba4e18a1d4b41c0d4de8fc

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting residue was purified by preparatory HPLC (0.1% TFA-H2O/acetonitrile)

Procedimiento

To a solution of 2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-N-(piperidin-3-yl)pyrimidin-4-amine, 5b, (0.020 g, 0.058 mmol) in 1:1 mixture of CH2Cl2/pyridine (2 mL) was added propylisocyanate (0.005 mL, 0.058 mmol). The reaction mixture was stirred at room temperature for 12 hours. The resulting residue was purified by preparatory HPLC (0.1% TFA-H2O/acetonitrile) to afford the desired product, 196.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08829007B2uspto-grants-2014_09