HuagongsheHuagongshe Chemistry Print Report · For research reference only
Deoxycytidine → 5-Hydroxy-2'-deoxycytidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Deoxycytidine | HCID 13711 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Hydroxydeoxycytidine-3',5'-diphosphate | HCID 131719392 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Hydroxy-2'-deoxycytidine | HCID 477413 | — |
Reaction Steps
5-Hydroxydeoxycytidine is synthesized in a similar manner to the published procedure of Eaton et al. (Biochim. Biophys. Acta 319:281-287, 1973) for 5-hydroxydeoxycytidine-3',5'-diphosphate. Bromine is added to a cooled (0° C.) solution of 2'-deoxycytidine (available from Sigma Chemical Company) in water until the yellow color persists. The excess bromine is quenched with cyclohexene and 2,4,6-collidine is added. After 2 hours, the reaction mixture is washed with ether and evaporated to dryness under vacuum. The crude 5-hydroxydeoxycytidine is then purified by reversed-phase HPLC on an Ultrasphere C18 column (Phenomenex) using a linear gradient of 0%-20% B in A (solvent A: 0.1 M NH4OAc, solvent B: 50% CH3CN in 0.1 M NH4OAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05512431 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-b77bb55e7142455189974ff8d13303fe |
| Source note | uspto-grants-1996_04 |