Reaktion #510147

ord-0543cc425b2343e9b8736a9425e4746d

Reaktionsgleichung

C[C@@H](O)[C@H](N)C(=O)O
threonine
CCN(C(C)C)C(C)C
DIEA
O=C(O)c1ccc(C#Cc2ccccc2)cc1
4-phenylethynyl-benzoic acid
O=C(O)c1ccc(C#Cc2ccccc2)cc1
4-Phenylethynyl-benzoic acid
CCN(C(C)C)C(C)C
DIEA
COC(=O)C(NC(=O)c1ccc(C#Cc2ccccc2)cc1)C(C)O
white solid
Ausbeute 99.1%
COC(=O)C(NC(=O)c1ccc(C#Cc2ccccc2)cc1)C(C)O
3-Hydroxy-2-(4-phenylethynyl-benzoylamino)-butyric acid methyl ester
Ausbeute 99.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 0.5M HCl (2×60 ml), sat. aq. NaHCO3 (60 ml), 50% diluted brine (60 ml), sat. brine (60 ml)
  2. 2
    Trocknendried with Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated under reduced pressure
  5. 5
    SonstigeUpon drying in vacuo

Vorschrift

A solution of threonine (1.66 g, 9.8 mmol) and DIEA (1.53 ml, 8.8 mmol) in DMF (10 ml) was added to a stirred solution of 4-phenylethynyl-benzoic acid 3 (1.55 g, 7.0 mmol) and DIEA (1.53 ml, 8.8 mmol) in DMF (11 ml) at rt. After 12 h, the reaction was diluted with EtOAc (300 ml) and washed with 0.5M HCl (2×60 ml), sat. aq. NaHCO3 (60 ml), 50% diluted brine (60 ml), sat. brine (60 ml), dried with Na2SO4, filtered and concentrated under reduced pressure. Upon drying in vacuo, 2.34 g of white solid was obtained (approximately quantitative yield in 99% purity).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08101640B2uspto-grants-2012_01