Réaction #40721

ord-6fb4034ab5794639bdf2ce1d1d5c13ae

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas refluxed for one hour
  2. 2
    AutreThe reaction mixture was evaporated to dryness
  3. 3
    Autrethe residue was recrystallized from benzene

Mode opératoire

As shown in FIG. 5, a mixture of 40 g (0.27 mole) of 3,6-dichloropyridazine and 40 mL of 80% hydrazine hydrate in 80 mL of ethanol was refluxed for one hour. The reaction mixture was evaporated to dryness and the residue was recrystallized from benzene to give 39 g of 1-(6-chloropyridazin-3-yl)hydrazine (compound 1003) (see Takahayashi, J. Pharm. Soc. Japan 75:778-781, 1955).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07728017B2uspto-grants-2010_06