تفاعل #1375812

ord-a227984b76c54b8b8b53c4bf308ad3aa

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGit is stirred for another three hours
  2. 2
    أخرىThe organic phase is separated
  3. 3
    أخرىdried on magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated by evaporation
  6. 6
    أخرىThe oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine
  7. 7
    تركيزThe product fractions are concentrated by evaporation in a vacuum
  8. 8
    أخرىdried

الإجراء التجريبي

13.2 g (30 mmol) of N-benzyl-2-(4-hydroxybenzyl)-3-azaglutaric acid-di-tert-butyl ester (Example b) is dissolved in 50 ml of anhydrous N,N-dimethylformamide and mixed at 0° C. under argon with 1.31 g (33 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 15 minutes, then 8.05 g (51.7 mmol) of ethyl iodide is added, the reaction temperature is allowed to increase to room temperature and it is stirred for another three hours. For working-up, the batch is taken up in toluene and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine. The product fractions are concentrated by evaporation in a vacuum and dried.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05746995uspto-grants-1998_05