Reaktion #457050

ord-a7fdcdfde8954e6ca1f98e088293533d

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture is concentrated by evaporation
  2. 2
    workup.DISSOLUTIONthe residue is dissolved in THF
  3. 3
    Einengenconcentrated by evaporation again
  4. 4
    Filtrationfiltered

Vorschrift

95 mg (0.30 mmol) of 4-(3-chloro-anilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidine in 1 ml of (3-methyl-but-1-yl)-amine are heated at 80° C. for 12 hours. The reaction mixture is concentrated by evaporation, the residue is dissolved in THF, concentrated by evaporation again, stirred with diethyl ether and filtered, yielding the title compound; m.p. 304-306° C.; FAB-MS: (M+H)+ =358.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06140332uspto-grants-2000_10