Ammonium formate → Gabapentin Enacarbil

HRID 30518

Reaktionsgleichung

Reaktionsgleichung von HRID 30518
C([O-])=O.[NH4+].[C:5]([O:10][CH:11]([O:13][C:14]([NH:16][CH2:17][C:18]1([CH2:24][C:25]([O:27]CC=C)=[O:26])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)=[O:15])[CH3:12])(=[O:9])[CH:6]([CH3:8])[CH3:7]>C(O)C.[Pd]>[C:5]([O:10][CH:11]([O:13][C:14]([NH:16][CH2:17][C:18]1([CH2:24][C:25]([OH:27])=[O:26])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)=[O:15])[CH3:12])(=[O:9])[CH:6]([CH3:8])[CH3:7]

Komponenten

5

Versuchsvorschrift

To a stirred suspension of ammonium formate (3.4 g, 54 mmol) in ethanol (34 mL), was added compound (15) (10 g, 27 mmol) together with 10% Pd/C (1 g) under a nitrogen atmosphere. After one hour, the reaction mixture was filtered and the catalyst washed with ethanol (2×10 mL). The filtrates were combined and evaporated. The crude product was dissolved in diethyl ether (150 mL) and the organic phase was washed with 2N HCl (100 mL), water (100 mL) and brine (100 mL). The ether layer was dried over anhydrous sodium sulfate and concentrated to give a viscous liquid that crystallized upon standing. The product was recrystallized using 1:10 ethyl acetate:heptane (100 mL) to give the product (11) as a white, crystalline solid (7.9 g, 88%), m.p 63-64° C.

Aufarbeitung

  1. filtrationthe reaction mixture was filtered
  2. washthe catalyst washed with ethanol (2×10 mL)
  3. customevaporated
  4. dissolutionThe crude product was dissolved in diethyl ether (150 mL)
  5. washthe organic phase was washed with 2N HCl (100 mL), water (100 mL) and brine (100 mL)
  6. dry with materialThe ether layer was dried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customto give a viscous liquid that
  9. customcrystallized
  10. customThe product was recrystallized

Quellen und Nachweise

ORD-Eintrag
ord-191ae72a0ffa4cf7a192af7f165a1881
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07423169B2

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