Reaktion #1702032

ord-170cc3a8259f48feaeec895636c2ce05

Reaktionsgleichung

CCc1c2c(nc3ccc(OC(=O)N4CCC(N5CCCCC5)CC4)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC.Cl.O.O.O
irinotecan hydrochloride trihydrate
[Na]
sodium
N[C@@H](CS(=O)(=O)O)C(=O)O
cysteic acid
CCc1c2c(nc3ccc(OC(=O)N4CCC(N5CCCCC5)CC4)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC
irinotecan

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated in vacuo
  2. 2
    workup.ADDITION100 ml of water was added to the residue
  3. 3
    Sonstigeobtained
  4. 4
    Sonstigeafter evaporation
  5. 5
    Sonstigetransparent (approx. 30 min)
  6. 6
    FiltrationThe obtained solution was filtered through 0.2 mm
  7. 7
    Filtrationfilter
  8. 8
    Sonstigefreeze dried
  9. 9
    FiltrationThe filtration

Vorschrift

Methanol stock-solutions of irinotecan hydrochloride trihydrate (100 ml, 1.15 mg/ml) and sodium salt of methyl ester of N-all-trans-retinoyl cysteic acid (27 ml, 15 mg/ml) were mixed in a 500 ml round-bottom flask and evaporated in vacuo. 100 ml of water was added to the residue obtained after evaporation and the mixture was stirred until it became clear and transparent (approx. 30 min). The concentration of irinotecan in the obtained solution was 1 mg/ml, corresponding to an irinotecan hydrochloride trihydrate concentration of 1.15 mg/ml. The obtained solution was filtered through 0.2 mm filter and freeze dried. The filtration did not result in reduction of irinotecan concentration.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765173B2uspto-grants-2014_07