HuagongsheHuagongshe Chemistry Print Report · For research reference only
3'-Azido-2',3'-dideoxyuridine 5'-monophosphate → Uridine 5'-(tetrahydrogen triphosphate), 3'-azido-2',3'-dideoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3'-Azido-2',3'-dideoxyuridine 5'-monophosphate | HCID 159486 | — |
| Reactant | Imidazolate | HCID 3386966 | — |
| Reactant | Triphosphate | HCID 3440921 | — |
| Reactant | Tributyl ammonium pyrophosphate | HCID 21910867 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Uridine 5'-(tetrahydrogen triphosphate), 3'-azido-2',3'-dideoxy- | HCID 451665 | — |
Reaction Steps
The triphosphate can be prepared according to the procedure of Hoard et al., J. Am. Chem. Soc., 87(8), 1785-1788 (1965). For example, 3'-azido-2',3'-dideoxyuridine monophosphate is activated (by making a imidazolide, according to methods known to those skilled in the art) and treated with tributyl ammonium pyrophosphate in DMF. The reaction gives primarily 3'-azido-2',3'-dideoxyuridine triphosphate, with some unreacted monophosphate and some diphosphate. Purification by anion exchange chromatography of a DEAE column is followed by isolation of CS-87 triphosphate, e.g., as the tetrasodium salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916122 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-f23db0f896d64f78a09450647c35ca1c |
| Source note | uspto-grants-1990_04 |