Reaktion #45078

ord-0f67b3a1d1344487a36595d5896f6113

Reaktionsgleichung

O=C([O-])[O-]
carbonate
COc1cc(COc2cc(N)[nH]n2)cc(OC)c1.Cl
5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine hydrochloride
COc1cc(COc2cc(N)[nH]n2)cc(OC)c1
5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine
Ausbeute 67.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction mixture was filtered
  2. 2
    WaschenMP carbonate was washed with 10% MeOH in DCM
  3. 3
    SonstigeThis was evaporated to dryness

Vorschrift

MP carbonate (2.74 mmol/g) (12.00 g, 32.88 mmol) was added to 5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine hydrochloride (5 g, 17.50 mmol) in methanol (200 mL) and water (20 mL). The resulting suspension was stirred at room temperature for 18 h. The reaction mixture was filtered and MP carbonate was washed with 10% MeOH in DCM. This was evaporated to dryness to afford 5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine (2.94 g, 67.5%) as an orange waxy solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737149B2uspto-grants-2010_06