Acetic Acid → 4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acid

HRID 221860

Reaktionsgleichung

Reaktionsgleichung von HRID 221860
[CH3:1][C:2]([CH3:9])([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].[NH:10]([C:12]1[CH:20]=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[CH:14][CH:13]=1)[NH2:11].C(O)(=O)C>CCO.C1COCC1>[NH2:6][C:5]1[N:10]([C:12]2[CH:13]=[CH:14][C:15]([C:16]([OH:18])=[O:17])=[CH:19][CH:20]=2)[N:11]=[C:3]([C:2]([CH3:9])([CH3:8])[CH3:1])[CH:4]=1

Komponenten

5

Versuchsvorschrift

A mixture of 4,4-dimethyl-3-oxo-pentanenitrile (4.52 g, 36.15 mmol), 4-hydrazinobenzoic acid (5.00 g, 32.86 mmol), and acetic acid (2 mL) in EtOH/THF (1:1) was refluxed for 16 h. After cooling, the solvent was concentrated at reduced pressure, and the crude was re-dissolved in EtOAc. The organic layer was washed with aqueous saturated Na2CO3 solution and brine, dried over MgSO4, filtered, and concentrated to half its volume. The resulting residue was filtered, and the solids were washed with cold EtOAc and dried under high vacuum to afford the title compound as a white solid (8.4 g, 99%). 1H-NMR (DMSO-d6) δ 12.91 (s, 1H), 7.99 (d, J=6.0 Hz, 2H), 7.75 (d, J=9.0 Hz, 2H), 5.42 (s, 1H), 5.39 (s, 2H), 1.21 (s, 9H); MS LC-MS [M+H]+=260, RT=1.83 min.

Aufarbeitung

  1. temperaturewas refluxed for 16 h
  2. temperatureAfter cooling
  3. concentrationthe solvent was concentrated at reduced pressure
  4. dissolutionthe crude was re-dissolved in EtOAc
  5. washThe organic layer was washed with aqueous saturated Na2CO3 solution and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated to half its volume
  9. filtrationThe resulting residue was filtered
  10. washthe solids were washed with cold EtOAc
  11. customdried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-61257910ddf04c16842a9415e8734b1b
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08207166B2

Verknüpfte Notizen

Wird geladen…