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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376448Generated: October 30, 2026

Thymidine → HCID 67703984, compound

https://huagongshe.com/reaction/1376448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 67703958HCID 67703958—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 67703984HCID 6770398456%

Reaction Conditions

Temperature45 °C

Reaction Steps

2-Amino-6-methylpropylamino-9H-purine (0.54 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 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 8 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 (92:8). Solvent was removed and lyophilization yielded 2-amino-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-(methylpropylamino)-9H-purine (0.40 g, 56%): mp 80°-84° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663154
Source datasetuspto-grants-1997_09
ORD IDord-b569375954314fbe952f85c95f03c001
Source noteuspto-grants-1997_09