Reacción #1144

ord-2e59b47848294fe195989e641f0b30fb

Ecuación de reacción

Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCC#N)oc2c1
2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran
[N-]=[N+]=[N-].[Na+]
sodium azide
[Cl-].[NH4+]
ammonium chloride
CN(C)C=O
N,N-dimethylformamide
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCc3nnn[nH]3)oc2c1
5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole
Rendimiento 78.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ethyl acetate
  2. 2
    LavadoAfter the ethyl acetate layer was washed with water
  3. 3
    Secadodried (MgSO4)
  4. 4
    workup.DISTILLATIONthe solvent was distilled off
  5. 5
    LavadoFrom the fraction eluted with methanol-chloroform (5:95

Procedimiento

A mixture of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.20 g), sodium azide (1.09 g), ammonium chloride (0.90 g) and N,N-dimethylformamide (30 ml) was stirred at 130° to 140° C. for 16 hours. The reaction mixture was poured over water and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform (5:95, v/v), 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole (1.05 g, 78%) was obtained, which was then recrystallized from dichloromethane-methanol to yield colorless prisms having a melting point of 177° to 178° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723479uspto-grants-1998_03