Réaction #1447087

ord-425c3f912f8c4000929b4ad0f7f79f3f

Équation de réaction

Cc1ccc(S(=O)(=O)O)cc1.N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1
D-Homophenylalanine Benzyl ester Tosylate
O=C([O-])O.[Na+]
sodium bicarbonate
N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1
D-Homophenylalanine Benzyl ester

Conditions de réaction

Température
25°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ExtractionThe water layer was extracted with ethyl acetate (3×10 mL)
  2. 2
    ExtractionThe combined organic extract
  3. 3
    Séchagewas dried over anhydrous sodium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated to dryness

Mode opératoire

D-Homophenylalanine Benzyl ester Tosylate (2.48 g, 5.6 mmol) was suspended in ethyl acetate (25 mL) and a saturated solution of sodium bicarbonate in water was added in portions (25 mL) with stirring at 25° C. The water layer was extracted with ethyl acetate (3×10 mL). The combined organic extract was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to afford D-Homophenylalanine Benzyl ester. The ester was dissolved in acetonitile (25 mL). NαNδ-bis-Boc-L-Ornithine (2.0 g, 6.0 mmol) was then added followed by N-hydroxysuccinimide (50 mg) and dicyclohexylcarbodiimide (1.28 g, 6.2 mmol). The reaction was stirred at 25° C. for 30 hr. filtered and the filtrate concentrated to dryness to afford crude product. It was purified by column chromatography on silica gel (hexane:ethyl acetate=3:1), which gave the title product (2.80 g) as white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07879795B2uspto-grants-2011_02