Réaction #47545

ord-bf470c71001d4023b15de42f30ce4a1d

Équation de réaction

COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2)=CC1=O
(S)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid methyl ester
[Li+].[OH-]
lithium hydroxide
O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2)=CC1=O
(S)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid
Rendement 86.0%

Conditions de réaction

Température
23°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

To a stirred solution of (S)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid methyl ester (340 mg, 0.9 mmol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (118 mg, 2.7 mmol). 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)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid (280 mg, 86%) as an off-white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07741327B2uspto-grants-2010_06