Potassium Carbonate → 5-(1,3-Oxazol-2-yl)-1-azabicyclo[3.2.1]octane oxalate salt

HRID 654527

Reaktionsgleichung

Reaktionsgleichung von HRID 654527
[N:1]12[CH2:8][C:5]([C:9]([NH2:11])=[O:10])([CH2:6][CH2:7]1)[CH2:4][CH2:3][CH2:2]2.[C:12]1(=O)[O:16][CH:15]=[CH:14][O:13]1.[C:18](=[O:21])([O-:20])[O-].[K+].[K+]>CCOCC>[C:12]([OH:16])(=[O:13])[C:18]([OH:20])=[O:21].[O:10]1[CH:15]=[CH:14][N:11]=[C:9]1[C:5]12[CH2:8][N:1]([CH2:7][CH2:6]1)[CH2:2][CH2:3][CH2:4]2

Komponenten

5

Versuchsvorschrift

A stirred mixture of 1-azabicyclo[3.2.1]oct-5-ylcarboxamide (D20, 1.50 g, 0.0097 mole) and vinylene carbonate (1.2 g, 0.014 mole) in polyphosphoric acid (35 g) was heated at 120°-130° C. for 2h. The reaction mixture was allowed to cool, then treated with ice, before basifying with potassium carbonate solution. The aqueous was shaken well with ether, then the mixture filtered and the organic layer separated. The aqueous was again extracted with ether (2×80 ml) and all the ether extracts combined, dried (Na2SO4) and concentrated in vacuo to leave a yellow oil. This was chromatographed on a basic alumina column eluting with ethyl acetate and the material obtained converted to its oxalate salt and recrystallised from methanol/ether to give the title compound (E12) as a white solid (410 mg, 16%) m.p. 143°-145° C.

Aufarbeitung

  1. temperaturewas heated at 120°-130° C. for 2h
  2. temperatureto cool
  3. additiontreated with ice
  4. filtrationthe mixture filtered
  5. customthe organic layer separated
  6. extractionThe aqueous was again extracted with ether (2×80 ml) and all the ether
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customto leave a yellow oil
  10. customThis was chromatographed on a basic alumina column
  11. washeluting with ethyl acetate
  12. customthe material obtained
  13. customrecrystallised from methanol/ether

Quellen und Nachweise

ORD-Eintrag
ord-e74371503dec42b8bb8460ca93b88ad0
Quelldatensatz
uspto-grants-1992_07
Patentnummer
US05132316

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