Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | 2',3'-Dideoxy-3'-fluorouridine | HCID 162450 | — |
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | HCID 178508671 | HCID 178508671 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | HCID 67703970 | HCID 67703970 | 49% |
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
| 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-add2e756c7b04537af3a763b27a05eec |
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| Source note | uspto-grants-1997_09 |
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