Reaktion #63144

ord-3db3d2bd444c48ce94a338689e4a7c66

Reaktionsgleichung

COc1cc(C)nc(N)n1
2-amino-4-methoxy-6-methylpyrimidine
c1nc[nH]n1
1,2,4-triazole
C=O
formaldehyde
CC(=O)O
acetic acid
COc1cc(C)nc(NCn2cncn2)n1
4-methoxy-6-methyl-2-(1,2,4-triazol-1-ylmethylamino)pyrimidine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturis refluxed for 11/2 hours
  2. 2
    SonstigeFirst a clear solution forms, from which the reaction product precipitates in crystalline form after a time
  3. 3
    TemperaturAfter the reaction mixture has cooled
  4. 4
    Filtrationthe crystalline title compound is filtered with suction
  5. 5
    Sonstigedried

Vorschrift

With stirring, a mixture of 13.9 g (0.1 mole) of 2-amino-4-methoxy-6-methylpyrimidine, 7 g (0.1 mole) of 1,2,4-triazole, 9.4 g (0.11 mole) of aqueous 35% formaldehyde and 1 g of acetic acid in 100 ml of methanol is refluxed for 11/2 hours. First a clear solution forms, from which the reaction product precipitates in crystalline form after a time. After the reaction mixture has cooled, the crystalline title compound is filtered with suction and dried. Yield: 14 g. Melting point: 191°-193° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04764203uspto-grants-1988_08