Reacción #161735

ord-f498d6096553424e9a7627d278a1d9ee

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with DCM
  2. 2
    OtroThe organic phase was dried
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated to dryness by rotary evaporation
  5. 5
    Filtraciónfiltered
  6. 6
    Otrodried

Procedimiento

0.20 g (0.73 mmol) 7-methoxy-3-piperidin-4-yl-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one and 0.14 mL (0.80 mmol) DIPEA were placed in 3.0 mL DMF. 0.17 g (0.74 mmol) tert. butyl 6-chloro-5-methyl-pyrimidine-4-carboxylate were added and the reaction mixture was stirred for 3 h at RT. The reaction mixture was mixed with water and extracted with DCM. The organic phase was dried, filtered and concentrated to dryness by rotary evaporation. The residue was combined with diisopropylether and the precipitated solid was suction filtered and dried.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08829006B2uspto-grants-2014_09