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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736052Generated: October 25, 2026

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

https://huagongshe.com/reaction/1736052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUridineHCID 6029—
ReactantUracil ArabinosideHCID 18323—
Reactant2-Amino-6-iodopurineHCID 6101575—
ReactantPotassium azideHCID 10290740—
SolventPotassium Phosphate, TribasicHCID 62657—
Product9-beta-D-arabinofuranosyl-2-amino-6-iodo-9H-purineHCID 5380200611%

Reaction Conditions

Temperature37 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539098
Source datasetuspto-grants-1996_07
ORD IDord-1a1e16ea95be46ec8a9d3c0d42803855
Source noteuspto-grants-1996_07