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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376452Generated: October 31, 2026

Thymidine → HCID 67569836, compound

https://huagongshe.com/reaction/1376452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 178508572HCID 178508572—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 67569836HCID 6756983670.6%

Reaction Conditions

Temperature45 °C

Reaction Steps

2-Amino-6-azetidinyl-9H-purine (0.50 g, 2.6 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.71 g, 3.1 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 7 days, 170 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 (7:3). Fractions containing product were pooled, concentrated, and flash chromatographed a second time on silica gel (2.5×20 cm) with dichloromethane:methanol (96:4). Solvent was removed and lyophilization yielded 0.566 g of 2-amino-6-azetidinyl-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-9H-purine (68%): mp 127°-129° C.; TLC Rf 0.70 (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-272be530f5584034995941f9250cf1b7
Source noteuspto-grants-1997_09