Reaktion #214389

ord-b760dad965544ee88f1830d2420b59e9

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux for 20 hours
  2. 2
    Sonstigeevaporated to dryness
  3. 3
    SonstigeThe residue was recrystallised from a mixture of ethanol and 2-propanol

Vorschrift

A mixture of 2-[2-(5-methyl-4-imidazolylmethylthio) ethylamino]-5-(4-methoxy-2-pyridylmethyl)-4-pyrimidone (0.97 g) and aqueous hydrobromic acid (48%, 20 ml) was boiled under reflux for 20 hours and evaporated to dryness. The residue was recrystallised from a mixture of ethanol and 2-propanol to give 2-]2-(5-methyl-4-imidazolylmethylthio) ethylamino]-5-(4-hydroxy-2-pyridylmethyl)-4-pyrimidone trihydrobromide, m.p. 167-169°. On recrystallisation from a mixture of ethanol and 2-propanol the melting point of the sample was lower owing to loss of hydrogen bromide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04255428uspto-grants-1981_03