Reaktion #64807

ord-3924147480804996801bcf6c30d00e9a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Sonstigethe reaction was quenched with water
  3. 3
    SonstigeThe layers were separated
  4. 4
    Extraktionthe aqueous layer was extracted with methylene chloride (2×)
  5. 5
    TrocknenThe combined organic extracts were dried (MgSO4)
  6. 6
    Sonstigeevaporated
  7. 7
    Sonstigeto give 2.82 g

Vorschrift

To a solution of N-[(phenylmethoxy)carbonyl]-L-leucine (3 g., 11.3 mmol.) in 60 mL of methylene chloride at -20° under argon was added N-methyl -morpholine (1.24 mL, 11.3 mmol.) followed by isobutylchloroformate (1.47 mL, 11.3 mmol.). The resulting suspension was stirred at -20° C. for 15 minutes at which time a solution of ammonia/methanol (about 5.6M, 20 mL, 113 mmol.) was added. After 30 minutes at -20° C., the reaction was quenched with water and warmed to room temperature. The layers were separated and the aqueous layer was extracted with methylene chloride (2×). The combined organic extracts were dried (MgSO4) and evaporated to give 2.82 g. of the title A compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05414017uspto-grants-1995_05