Reacción #480480

ord-fd40204fe0fd4cae9da61a2ce2d7ae93

Disolventes

Condiciones de reacción

Temperatura
105°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe cooled reaction mixture
  2. 2
    Filtraciónfiltered through a short pad of diatomaceous earth
  3. 3
    Concentraciónwas concentrated under reduced pressure
  4. 4
    OtroThe residue was purified by flash chromatography (Hexane:EtOAc, 1:1)

Procedimiento

A degassed mixture of 11-ethyl-5,11-dihydro-8-[2-(4-amino-2-methylphenoxy)ethyl]-5-methyl-6H-dipyrido[3,2-b:2′,3′-e][1,4]diazepin-6-one (100 mg, 0.25 mmol), ethyl 4-bromobenzoate (61.0 μL, 0.37 mmol), t-BuONa (36.0 mg, 0.37 mmol), Pd2(dba)3 (2.5 mg, 2.7 μmol) and (+/−)-BINAP (5.0 mg, 8.0 1mol) in toluene (8 mL) was heated to 105° C. under nitrogen for 48 h. The cooled reaction mixture was diluted with EtOAc, filtered through a short pad of diatomaceous earth and was concentrated under reduced pressure. The residue was purified by flash chromatography (Hexane:EtOAc, 1:1) to give the title compound (55 mg, 40% yield) as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06806265B2uspto-grants-2004_10