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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333487Generated: October 29, 2026

Thymidine → HCID 6481573, compound

https://huagongshe.com/reaction/333487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
ReactantHCID 67113788HCID 67113788—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 6481573HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877905B2
Source datasetuspto-grants-2014_11
ORD IDord-70cca1d7f6a044f294d4f24365e5c16a
Source noteuspto-grants-2014_11