Reaktion #549548

ord-449a1159b8ac4da49d12d0f8ec5647ea

Reaktionsgleichung

CC(C)(C)c1cc(N)[nH]n1
3-tert.-butyl-5-amino-1H-pyrazole
COc1cccc(OC)c1C(=O)Cl
2,6-dimethoxybenzoyl chloride
COc1cccc(OC)c1C(=O)Nc1cc(C(C)(C)C)n[nH]1
N-[3-(1,1-dimethylethyl)-1H-pyrazol-5-yl]-2,6-dimethoxybenzamide
Ausbeute 18.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was heated
  2. 2
    Temperaturat reflux for sixteen hours
  3. 3
    TemperaturThe reaction mixture was then cooled
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigethe solvent was removed from the filtrate by evaporation
  6. 6
    SonstigeThe residue was crystallized from ethyl acetate

Vorschrift

To a stirred solution of 1.39 g of 3-tert.-butyl-5-amino-1H-pyrazole in 50 ml of benzene were added in one portion 2.01 g of 2,6-dimethoxybenzoyl chloride. The reaction mixture was heated at reflux for sixteen hours. The reaction mixture was then cooled, filtered, and the solvent was removed from the filtrate by evaporation. The residue was crystallized from ethyl acetate to provide 550 mg of N-[3-(1,1-dimethylethyl)-1H-pyrazol-5-yl]-2,6-dimethoxybenzamide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04515625uspto-grants-1985_05