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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376455Generated: October 31, 2026

Thymidine → HCID 67703970, compound

https://huagongshe.com/reaction/1376455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 178508671HCID 178508671—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 67703970HCID 6770397049%

Reaction Conditions

Temperature45 °C

Reaction Steps

2-Amino-6-phenylamino-9H-purine (0.63 g, 2.7 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.50 g, 2.2 mmoles) 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 2 days, 100 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:methanol (97:2:1). Fractions containing product were combined and flash chromatographed on a second silica gel column (2.5×20 cm) with hexane:acetone (6:4). Solvent was removed and lyophilization yielded 0.364 g of 2-amino-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-phenylamino-9H-purine (49%): mp 193°-194° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663154
Source datasetuspto-grants-1997_09
ORD IDord-add2e756c7b04537af3a763b27a05eec
Source noteuspto-grants-1997_09