Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1736052Erstellt: 24. Oktober 2026

Uridine → 9-beta-D-arabinofuranosyl-2-amino-6-iodo-9H-purine

https://huagongshe.com/de/reaction/1736052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktUridineHCID 6029—
EduktUracil ArabinosideHCID 18323—
Edukt2-Amino-6-iodopurineHCID 6101575—
EduktPotassium azideHCID 10290740—
LösungsmittelPotassium Phosphate, TribasicHCID 62657—
Produkt9-beta-D-arabinofuranosyl-2-amino-6-iodo-9H-purineHCID 5380200611%

Reaktionsbedingungen

Temperatur37 °C

Reaktionsschritte

2-Amino-6-iodopurine (Sigma Chemicals, St. Louis. Mo.) (25.5 mmoles, 6.75 g) and uracil arabinoside (61.9 mmoles. 15.1 g) were combined in 0.31 liters of 10 mM potassium phosphate pH 6.9 with 0.02% potassium azide. Purified purine nucleoside phosphorylase (17000 units) and uridine phosphorylase (2000 units) were added and the solution stirred at 37° C. After 18 days an additional 5700 units of uridine phosphorylase were added. Fifty-seven days later the reaction was filtered and the flitrate chromatographed on a column containing XAD-2 resin (8×11 cm). The product was eluted with a step gradient of ethanol/water (v/v) as follows: 0.35 liter 10%; 1 liter 20%; 1 liter 50%; 0.2 liter 95%. Product-containing fractions were combined and the ethanol removed under vacuum. The residue was dissolved in 30% n-propanol/water (v/v) and chromatographed on a 7.5×90 cm column containing BioRad P-2 resin, This procedure yielded 1.1 g of 9-β-D-arabinofuranosyl-2-amino-6-iodo-9 H-purine as a 0.5 hydrate. NMR and mass spectrometry were consistent with the structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05539098
Quelldatensatzuspto-grants-1996_07
ORD IDord-1a1e16ea95be46ec8a9d3c0d42803855
Quellennotizuspto-grants-1996_07