HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thymidine → HCID 6481573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | HCID 67113788 | HCID 67113788 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 6481573 | HCID 6481573 | — |
Reaction Steps
To a solution of 5-benzyloxy-2′-deoxyuridine (10 mg) in ethanol (1 mL) was added Pd/C (10%, 10 mg), and the mixture was stirred for five minutes. Hydrogen was introduced to the system via a balloon and the reaction mixture was stirred at room temperature. Aliquots (5 μL) were taken out from the reaction mixture at various time point intervals and were analyzed by thin layer chromatography and HPLC. Complete cleavage to thymidine was observed after ten minutes at room temperature (Scheme 42 and FIG. 4). The intermediate of the cleavage was identified to be 5-hydroxymethyl-dU generated from initial removal of benzyl group, and HOMedU was further reduced to thymidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877905B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-70cca1d7f6a044f294d4f24365e5c16a |
| Source note | uspto-grants-2014_11 |