Réaction #657320

ord-32df2614b91f4eb19b253315662d9639

Solvants

Conditions de réaction

Température
110°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with dichloromethane (3×100 mL)
  2. 2
    SéchageThe organic layer is dried over anhydrous magnesium sulphate
  3. 3
    Filtrationfiltered
  4. 4
    Concentrationconcentrated under reduced pressure
  5. 5
    AutreThe crude material is purified by column chromatography

Mode opératoire

To a solution of 4-bromo-3-phenyl-1H-pyrazole-5-amine (5.0 g, 0.02 mol) in acetic acid (50 mL) is added 1,1,3,3-tetramethoxypropane (4.14 g, 0.025 mol). The mixture is stirred at 110° C. for 1 h. The reaction mixture is then poured into water, basified with NH4OH and extracted with dichloromethane (3×100 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in dichloromethane and ethyl acetate (1:0 to 95:5) as eluent and 4.2 g (75%) of 3-bromo-2-phenylpyrazolo[1,5-a]pyrimidine are obtained as a beige solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09023844B2uspto-grants-2015_05