Reaktion #61101

ord-812e66f511de4271aab6d20fc643c8cf

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepartitioned between ethyl acetate and water
  2. 2
    SonstigeThe organic layer was separated
  3. 3
    Trocknendried over sodium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    SonstigeThe residue was purified by chromatography over silica gel gradient
  7. 7
    Wascheneluted with 0-100% ethyl acetate in hexanes
  8. 8
    Sonstigethe isolated material further purified by preparative thin layer chromatography
  9. 9
    Wascheneluted with ethyl acetate
  10. 10
    SonstigePrecipitation of the isolated product from dichloromethane with an excess of hexanes

Vorschrift

Crude (2S,3S)-2-{(R)-2-amino-2-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-acetylamino}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide (≈0.19 mmol) was dissolved in tetrahydrofuran (10 mL) that contained diisopropylethylamine (160 μL, 122 mg, 0.94 mmol) and was transferred via cannula to a solution of diphosgene (16 μL, 26 mg, 0.13 mmol) in tetrahydrofuran (15 mL) at 0° C. The reaction mixture was stirred for 20 minutes and then partitioned between ethyl acetate and water. The organic layer was separated and dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography over silica gel gradient eluted with 0-100% ethyl acetate in hexanes and the isolated material further purified by preparative thin layer chromatography using silica gel eluted with ethyl acetate. Precipitation of the isolated product from dichloromethane with an excess of hexanes gave (2S,3S)-2-{4-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide as an off white solid (32 mg, 29%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07427635B2uspto-grants-2008_09