Reaktion #367206

ord-ee844c9e1e39460ab48420f682fe5156

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction was cooled
  2. 2
    TemperaturAfter continued reflux
  3. 3
    Sonstigethe product crystallized from the cooled reaction mixture
  4. 4
    FiltrationFiltration
  5. 5
    Waschenwash (2 L)

Vorschrift

2-(7,8-Dimethoxy-2H-1-benzopyran-5-ylmethyl)-3-morpholino acrylonitrile (562 g, 1.64 mol) and aniline hydrochloride (234 g, 1.80 mol) were refluxed in SD3A (2.4 L) for one hour. The reaction was cooled, and guanidine hydrochloride (313 g, 3.28 mol) and sodium methoxide (275 g, 5.08 mol) were added. After continued reflux, the product crystallized from the cooled reaction mixture. Filtration followed by water wash (2 L) gave 2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine (220 g, 42.7%). Crystallization from ethanol-water gave title compound, mp 235°-238°, identical to the product of Example 1C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04587342uspto-grants-1986_05