Reaktion #742277

ord-991cb4d205da4a15845a855934af0d9d

Reaktionsgleichung

CC(=O)c1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)O)cc1
Fmoc-4-acetyl-L-phenylalanine
C1CCNCC1
piperidine
CC(=O)c1ccc(C[C@H](N)C(=O)O)cc1
p-acetyl-L-phenylalanine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated
  2. 2
    Sonstigeto obtain white powder
  3. 3
    Filtrationthe supernatant was collected by filtration
  4. 4
    Sonstigeto separate the desired product from the reaction mixture (5-30% CH3CN in H2O with 0.1% TFA over 30 min)

Vorschrift

Fmoc-4-acetyl-L-phenylalanine was purchased from RSP Amino Acid Analogues, Inc. (Worcester, Mass.). This compound (1.0 g, 2.3 mmol) was stirred with 4 mL of piperidine (20% in DMF) for 2 hours at room temperature. The solvent was evaporated to obtain white powder. The solid was then resuspended in 10 mL of cold water (0.1% TFA), and the supernatant was collected by filtration. Preparative reverse-phase HPLC (Microsorb C18, Rainin Instrument Co., Inc., Woburn, Mass.) was used to separate the desired product from the reaction mixture (5-30% CH3CN in H2O with 0.1% TFA over 30 min). The eluant (tR=12 min) was lyophilized to a obtain white solid (0.45 g, 88%). 1HNMR (D2O): δ 7.85-7.28 (m, 4H), 4.23 (dd, 1H, 5.4 Hz), 3.2 (m, 2H), 2.7 (s, 3H). LRMS, calcd for C11H13NO3 (M++1): 208.09. Found (ESI): 208.47.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08071344B2uspto-grants-2011_12