Reaktion #47540

ord-505d1444decd43d4b77172dceea94ae5

Lösungsmittel

Reaktionsbedingungen

Temperatur
23°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenAfter this time, the mixture was concentrated
  2. 2
    workup.ADDITIONthe reaction mixture was diluted with water
  3. 3
    SonstigeThe reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation
  4. 4
    SonstigeThe precipitate was removed by filtration
  5. 5
    Waschenwashed with cold water
  6. 6
    Sonstigedried in vacuo

Vorschrift

To a stirred solution of (S)-3-cyclohexyl-2-[4-(3-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (1.10 g, 0.003 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (382 mg, 0.016 mol). The reaction mixture was stirred at 23° C. for 2 h. After this time, the mixture was concentrated and the reaction mixture was diluted with water. The reaction mixture was acidified with 2N hydrochloric acid, during which time precipitation occurred. The precipitate was removed by filtration, washed with cold water and dried in vacuo to obtain (S)-3-cyclohexyl-2-[4-(3-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid (920 gm, 87%) as an off-white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741327B2uspto-grants-2010_06