تفاعل #1375812
ord-a227984b76c54b8b8b53c4bf308ad3aa
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGit is stirred for another three hours
- 2أخرىThe organic phase is separated
- 3أخرىdried on magnesium sulfate
- 4ترشيحfiltered
- 5تركيزconcentrated by evaporation
- 6أخرىThe oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine
- 7تركيزThe product fractions are concentrated by evaporation in a vacuum
- 8أخرىdried
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.