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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376454Generated: November 3, 2026

Thymidine → HCID 86751193, compound

https://huagongshe.com/reaction/1376454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 67703983HCID 67703983—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 86751193HCID 8675119350%

Reaction Conditions

Temperature45 °C

Reaction Steps

6 Ethylmethylamino-9H-purine (0.46 g, 2.6 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.50 g, 2.2 moles) were suspended in 50 ml, 10 mM potassium phosphate buffer, pH 7.0, containing 0.04% potassium azide. 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 6 days, 150 ml MeOH 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 (9:1). Solvent was removed and lyophilization yielded 0.323 g of 9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-ethylmethylamino-9H-purine (50%): mp 99°-100° C.; TLC Rf 0.75 (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-4e3c31de414049b9b557090eb5bca3d4
Source noteuspto-grants-1997_09