Réaction #4425

ord-9fe523c9c62a46dba0a4c75868ed88c4

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was refluxed for 6 hours
  2. 2
    AutreThe reaction mixture was evaporated in vacuo
  3. 3
    AutreThe residue was chromatographed on silica gel

Mode opératoire

To a suspension of 2-chloro-3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidine (10.0 g) in chloroform (100 ml) was added hydrazine hydrate (3.66 ml). The mixture was refluxed for 6 hours. The reaction mixture was evaporated in vacuo. The residue was chromatographed on silica gel using chloroform to give 3,4-dihydro-6-(3,4-dimethoxyphenyl)-2-hydrazino-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidine (3.46 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04725600uspto-grants-1988_02