Hydrochloric Acid → 4-[4-Chloro-3-(1-cyclohexyl-2-oxo-pyrrolidin-3-ylmethyl)-2-fluoro-phenyl]-butyric acid

HRID 2235245Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2235245
[OH-].[Na+].C([O:5][C:6](=[O:31])[CH2:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([CH2:17][CH:18]2[CH2:22][CH2:21][N:20]([CH:23]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)[C:19]2=[O:29])[C:11]=1[F:30])C.Cl>CO>[Cl:16][C:13]1[CH:14]=[CH:15][C:10]([CH2:9][CH2:8][CH2:7][C:6]([OH:31])=[O:5])=[C:11]([F:30])[C:12]=1[CH2:17][CH:18]1[CH2:22][CH2:21][N:20]([CH:23]2[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]2)[C:19]1=[O:29]

Komponenten

5

Versuchsvorschrift

Add 5 N NaOH solution (3 mL, 3 mmol) into 4-[4-chloro-3-(1-cyclohexyl-2-oxo-pyrrolidin-3-ylmethyl)-2-fluoro-phenyl]-butyric acid ethyl ester (Preparation 79) (0.58 g, 1.4 mmol) in methanol (5 mL) at room temperature and stir for 30 minutes. Evaporate MeOH under reduced pressure and neutralize the residue by 1N HCl. Extract the mixture with ethyl acetate (10 mL) and separate the organic layer. Dry the organic layer with magnesium sulfate, filter and evaporate solvent under reduced pressure. Purify the residue by column chromatography to obtain the title product as white solid (300 mg, 55%): Mass spectrum (ion spray): m/z=396.0 (M+H).

Aufarbeitung

  1. extractionExtract the mixture with ethyl acetate (10 mL)
  2. customseparate the organic layer
  3. dry with materialDry the organic layer with magnesium sulfate
  4. filtrationfilter
  5. customevaporate solvent under reduced pressure
  6. customPurify the residue by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-fdb962f2302f4826b3d6a3482604c098
Quelldatensatz
uspto-grants-2010_05
Patentnummer
US07713979B2

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