Reacción #4627

ord-fe8a390673e842ac9509d98d9cab3091

Ecuación de reacción

CC(COc1ccc2c(c1)C(=O)NC(C)(C)O2)NCc1ccccc1
6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one
CNC(=O)c1ccc(OCC2CO2)cc1
4-(2,3-epoxypropoxy)-N-methylbenzamide
CNC(=O)c1ccc(OCC(O)CN(Cc2ccccc2)C(C)COc2ccc3c(c2)C(=O)NC(C)(C)O3)cc1
1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrohas been evaporated off
  2. 2
    OtroThe acidic, aqueous phase is separated off
  3. 3
    Temperaturawhilst cooling with ice
  4. 4
    Extracciónextracted with ethyl acetate
  5. 5
    OtroBy separating off
  6. 6
    Secadodrying (MgSO4)
  7. 7
    Concentraciónconcentrating the ethyl acetate
  8. 8
    Extracciónextract by evaporation

Procedimiento

A solution of 13.6 g of 6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one and 10.4 g of 4-(2,3-epoxypropoxy)-N-methylbenzamide in 80 ml of isopropanol is refluxed for 30 hours. The residue remaining after the solvent has been evaporated off is divided between ether and 2N hydrochloric acid. The acidic, aqueous phase is separated off, and, whilst cooling with ice, rendered alkaline with approximately 10% aqueous ammonia solution and extracted with ethyl acetate. By separating off, drying (MgSO4) and concentrating the ethyl acetate extract by evaporation, the crude 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol is obtained as an oil which may be used without further purification for catalytic debenzylation.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04727067uspto-grants-1988_02