Réaction #47501

ord-804da6caf2ac40b4b5d1ed9f6e552cfe

Équation de réaction

CCCc1ccccc1OC1=CC(=O)N([C@@H](CC2CCCCC2)C(=O)OC)C1
(S)-3-cyclohexyl-2-[2-oxo-4-(2-propyl-phenoxy)-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
[Li+].[OH-]
lithium hydroxide
CCCc1ccccc1OC1=CC(=O)N([C@@H](CC2CCCCC2)C(=O)O)C1
(S)-3-cyclohexyl-2-[2-oxo-4-(2-propyl-phenoxy)-2,5-dihydro-pyrrol-1-yl]-propionic acid
Rendement 106.3%

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-[2-oxo-4-(2-propyl-phenoxy)-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (440 mg, 0.001 mol) in tetrahydrofuran-water (3:1, 10 mL) was added lithium hydroxide (143 mg, 0.006 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-[2-oxo-4-(2-propyl-phenoxy)-2,5-dihydro-pyrrol-1-yl]-propionic acid (395 mg, 93%) as a yellow solid.

Source

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