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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376447Generated: October 31, 2026

Methanol → HCID 86751192, compound

https://huagongshe.com/reaction/1376447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2',3'-Dideoxy-3'-fluorouridineHCID 162450—
ReactantPotassium azideHCID 10290740—
ReactantHCID 67703971HCID 67703971—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 86751192HCID 8675119242%

Reaction Conditions

Temperature45 °C

Reaction Steps

2-Amino-6-ethylmethylamino-9H-purine (0.5 g, 2.6 mmoles) and 2',3'-dide-oxy-3'-fluorouridine (0.5 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 phosphory-lase (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, 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). Product containing fractions were again pooled, concentrated, and flash chromatographed on silica gel (2.5×20 cm) with dichloromethane:meth-anol (95:5). Solvent was removed and lyophilization yielded 9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofura-nosyl)-9H-purine (0.22 g, 32%): mp 89°-9° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663154
Source datasetuspto-grants-1997_09
ORD IDord-6cfa0fbfcacd4062a86d5b86c7530349
Source noteuspto-grants-1997_09