Reacción #81170

ord-20f45e438e07447e98a1a0251b75d53c

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe reaction mixture was stirred at room temperature for 2 hours
  2. 2
    workup.WAITat 60° C. for 4 hours
  3. 3
    Lavadothe solution was washed three times with water
  4. 4
    SecadoThe solution was then dried over anhydrous sodium sulfate
  5. 5
    workup.DISTILLATIONafter which it was freed from the solvent by distillation
  6. 6
    OtroThe residue was purified by column chromatography through silica gel
  7. 7
    workup.ADDITIONby volume mixture of hexane and ethyl acetate as the eluent

Procedimiento

48 mg of sodium hydride (as a 55% w/w dispersion in mineral oil) were added to a solution of 0.26 g of ethyl 4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylate (prepared as described in Preparation 9) in 5 ml of N,N-dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes. A solution of 0.72 g of 4-[2-(trityltetrazol-5-yl)phenyl]benzyl bromide in 5 ml of N,N-dimethylformamide was then added, and the reaction mixture was stirred at room temperature for 2 hours and then at 60° C. for 4 hours. At the end of this time, it was dissolved in ethyl acetate and the solution was washed three times with water. The solution was then dried over anhydrous sodium sulfate, after which it was freed from the solvent by distillation. The residue was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.62 g of the title compound as an amorphous solid. This was crystallized from diisopropyl ether, to give the title compound as crystals, melting at 167°-168° C. (with decomposition).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05616599uspto-grants-1997_04