Réaction #47550

ord-4cce9d6a80a548a693d0e0e2f0b6a1c4

Équation de réaction

COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(OC)c2)=CC1=O
(S)-3-cyclohexyl-2-[4-(3-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
[Li+].[OH-]
lithium hydroxide
COc1cccc(OC2=CC(=O)N([C@@H](CC3CCCCC3)C(=O)O)C2)c1
(S)-3-cyclohexyl-2-[4-(3-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
Rendement 62.1%

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)-3-cyclohexyl-2-[4-(3-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (1.12 g, 0.003 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (387 mg, 0.009 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-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid (670 mg, 62%) as a light yellow solid.

Source

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