Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | 2',3'-Dideoxy-3'-fluorouridine | HCID 162450 | — |
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | HCID 67703958 | HCID 67703958 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | HCID 67703984 | HCID 67703984 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663154 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-b569375954314fbe952f85c95f03c001 |
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| Source note | uspto-grants-1997_09 |
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