Reaktion #10005

ord-91c9829968e24bb3a557a7a85a8195ae

Reaktionsgleichung

CCn1cnc2c(Nc3cccc(F)c3)nc(Cl)nc21
2-chloro-9-ethyl-6-(3-fluoro-phenyl-amino)-9H-purine
CCn1cnc2c(Nc3cccc(F)c3)nc(NCCN)nc21.Cl
2-(2-Amino-ethyl-amino)-9-ethyl-6-(3-fluor-phenyl-amino)-9H-purine hydrochloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto cool
  2. 2
    WaschenThe organic phase is washed with water
  3. 3
    Sonstigeseparated off
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    SonstigeAfter removal of the solvent
  6. 6
    workup.DISSOLUTIONthe residue is dissolved in dioxane
  7. 7
    workup.ADDITIONtreated with 4 N HCl in dioxane

Vorschrift

0.2 g (0.62 mmol) of 2-chloro-9-ethyl-6-(3-fluoro-phenyl-amino)-9H-purine is stirred in 2.5 ml of ethylenediamine at 75° C. for 3 h, and the mixture is allowed to cool and is diluted with ethyl acetate. The organic phase is washed with water, separated off and dried over sodium sulfate. After removal of the solvent, the residue is dissolved in dioxane, and treated with 4 N HCl in dioxane. 2-(2-Amino-ethyl-amino)-9-ethyl-6-(3-fluor-phenyl-amino)-9H-purine hydrochloride is obtained as a crystalline precipitate by this procedure. This precipitate is filtered off and dried; m.p.>250° C.; FAB-MS: (M+H)+=315; Rf=0.6 (ethyl acetate:isopropanol:water:22% aqueous ammonium hydroxide solution=40:60:15:18).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091346B1uspto-grants-2006_08