Reaktion #1375820

ord-90253e2cfdb644428d10ee80793bbb7e

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenIt is concentrated by evaporation in a vacuum
  2. 2
    Sonstigeevaporated to dryness
  3. 3
    TemperaturThe residue is refluxed with 200 ml of methanol
  4. 4
    Filtrationthe undissolved material is filtered out
  5. 5
    Sonstigeevaporated to dryness in a vacuum
  6. 6
    workup.DISSOLUTIONthe residue is dissolved in 50 ml of water
  7. 7
    WaschenIt is eluted first with 0.5 l of water, which
  8. 8
    WaschenThen, it is eluted with 0.5 l of 0.5 N ammonia solution
  9. 9
    SonstigeIt is evaporated almost to dryness in a vacuum
  10. 10
    workup.ADDITIONmixed with 100 ml of water and enough cation exchanger IRC 50
  11. 11
    workup.ADDITIONis added
  12. 12
    FiltrationThe solution is then filtered
  13. 13
    Sonstigefreeze-dried

Vorschrift

3 g (8.66 mmol) of 1,4,7-tris-(carboxymethyl)-1,4,7, 10-tetraazacyclododecane is stirred in 50 ml of dimethylformamide for 10 hours with 1.83 g (10 mmol) of 1-bromo-3,6-dioxa-heptane, 100 mg of sodium iodide and 4 g of potassium carbonate at 90° C. It is concentrated by evaporation in a vacuum and the residue is spread between 100 ml of water and 50 ml of diethyl ether. The aqueous phase is adjusted to pH 2 with 5 N hydrochloric acid and evaporated to dryness. The residue is refluxed with 200 ml of methanol, the undissolved material is filtered out, evaporated to dryness in a vacuum, the residue is dissolved in 50 ml of water, adjusted to pH 2 with 5 N hydrochloric acid and the solution is put on a column with 200 ml of cation exchanger IRC 50. It is eluted first with 0.5 l of water, which is discarded. Then, it is eluted with 0.5 l of 0.5 N ammonia solution. It is evaporated almost to dryness in a vacuum, mixed with 100 ml of water and enough cation exchanger IRC 50 is added with stirring to reach pH 3.5. The solution is then filtered and freeze-dried. 2.95 g of the title compound with a water content of 3.5% is obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05747000uspto-grants-1998_05