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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376449Generated: October 28, 2026

Thymidine → HCID 9860968, compound

https://huagongshe.com/reaction/1376449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 178483098HCID 178483098—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 9860968HCID 986096826.1%

Reaction Conditions

Temperature45 °C

Reaction Steps

2-Amino-6-dimethylamino-9H-purine (0.46 g, 2.6 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.50 g, 2.2 mmoles) were suspended in potassium phosphate buffer (50 ml, 10 mM), pH 7.0, containing potassium azide 0.04%. Purine nucleoside phosphorylase (1120 I.U.) and thymidine phosphorylase (10,000 I.U.) (Krenitsky et al., Biochemistry, 20, 3615 (1981) and U.S. Pat. No. 4,381,344) immobilized on DEAE cellulose was added to the reaction and the suspension was stirred at 45° C. After 19 days, MeOH (170 ml) was added to the reaction. The reaction was applied to a column containing AG1-X2 (OH- form, 2.5×10 cm) and eluted with MeOH. Fractions containing product were pooled, concentrated, and flash chromatographed on silica gel (2.5×20 cm) with dichloromethane:acetone (88:12). Solvent was removed and lyophilization yielded 2-amino-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-(dimethylamino)-9H-purine 0.17 g (26%): mp 96°-100° C.; TLC Rf 0.79 (silica gel, MeCN: 15N NH4OH:H2O/85:5:10);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663154
Source datasetuspto-grants-1997_09
ORD IDord-1d28815844a24e739e27d043dc7015bc
Source noteuspto-grants-1997_09