Réaction #429435

ord-9cfc6da584024d33aab88257f5661b98

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecooled to 0° C.
  2. 2
    workup.STIRRINGAfter stirring at 0° C. for 1 hour and at room temperature for 2 hours
  3. 3
    Autrethe mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid
  4. 4
    Extractionsubsequently extracted three times with ethyl acetate
  5. 5
    LavageThe pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine
  6. 6
    Séchagedried (sodium sulfate)
  7. 7
    Filtrationfiltered
  8. 8
    Autreto give 5.77 g

Mode opératoire

A slurry of glycine, ethyl ester, hydrochloride salt (2.718 g, 19.5 mmol.) in dimethylformamide (36 ml.) was treated with 4-methyl morpholine (2.60 ml., 2.39 g., 23.6 mmol.) and stirred at room temperature for 5 minutes. The mixture was then treated with (S)-2-phthalimido-6-hydroxyhexanoic acid (4.50 g., 16.2 mmol.) and hydroxybenzotriazole (2.225 g., 16.5 mmol.), cooled to 0° C., and then treated with ethyl-3-(3-dimethylamino) -propyl carbodiimide, hydrochloride salt (3.438 g., 17.9 mmol.). After stirring at 0° C. for 1 hour and at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid and subsequently extracted three times with ethyl acetate. The pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine, then dried (sodium sulfate), filtered and stripped to give 5.77 g. of title product as a colorless oil. TLC (ethyl acetate) Rf =0.34.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05856477uspto-grants-1999_01