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Deoxycytidine → 5-Hydroxy-2'-deoxycytidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Deoxycytidine | HCID 13711 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | 5-Hydroxydeoxycytidine-3',5'-diphosphate | HCID 131719392 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-Hydroxy-2'-deoxycytidine | HCID 477413 | — |
反応手順
5-Hydroxydeoxycytidine is synthesized in a similar manner to the published procedure of Eaton et al. (Biochem. 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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06132776 |
| 出典データセット | uspto-grants-2000_10 |
| ORD ID | ord-a7c45c77dfa64da1ae9d570882b17a14 |
| 出典メモ | uspto-grants-2000_10 |