Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | 2',3'-Dideoxy-3'-fluorouridine | HCID 162450 | — |
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | HCID 178483098 | HCID 178483098 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | HCID 9860968 | HCID 9860968 | 26.1% |
Reaction Steps
2-Amino-6-dimethylamino-9H-purine (0.46 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 potassium azide 0.04%. 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 19 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 (88:12). Solvent was removed and lyophilization yielded 2-amino-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-(dimethylamino)-9H-purine 0.17 g (26%): mp 96°-100° C.; TLC Rf 0.79 (silica gel, MeCN: 15N NH4OH:H2O/85:5:10);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05663154 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-1d28815844a24e739e27d043dc7015bc |
|---|
| Source note | uspto-grants-1997_09 |
|---|