反応 #83234

ord-5245f4db94ff45ddaff1401dd3915f96

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was refluxed for 5 hours
  2. 2
    温度The reaction mixture was cooled
  3. 3
    濃縮concentrated in vacuo
  4. 4
    その他The residue was purified by column chromatography on silica gel
  5. 5
    その他the obtained oil was crystallized from a mixture of ethyl acetate and hexane

実験手順

A mixture of 5-amino-3-(4-fluorophenyl)-4-(pyridin-4-yl)pyrazole (254 mg) and 4-methyl-3-penten-2-one (5 ml) was refluxed for 5 hours. The reaction mixture was cooled and concentrated in vacuo. The residue was purified by column chromatography on silica gel and the obtained oil was crystallized from a mixture of ethyl acetate and hexane to give 6,7-dihydro-2-(4-fluorophenyl)-3-(pyridin-4-yl)-5,7,7-trimethylpyrazolo[1,5-a]pyrimidine (83 mg).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05624931uspto-grants-1997_04