Reaktion #83220

ord-74b0c6cafdd747a88b5d591665edad9a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe resulting clear solution was concentrated in vacuo
  2. 2
    workup.ADDITIONTo the residue was added ethanol (3 ml)
  3. 3
    Einengenthe solution was concentrated in vacuo
  4. 4
    SonstigeThe residue was crystallized from a mixture of ethanol and diethyl ether

Vorschrift

To a suspension of 2-(4-fluorophenyl)-3-(pyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (100 mg) in methanol (2 ml) was added 10% methanolic hydrogen chloride (0.5 ml). The resulting clear solution was concentrated in vacuo. To the residue was added ethanol (3 ml) and the solution was concentrated in vacuo. The residue was crystallized from a mixture of ethanol and diethyl ether to give 2-(4-fluorophenyl)-3-(pyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine dihydrochloride (100 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05624931uspto-grants-1997_04