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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157351Generated: October 25, 2026

Oxalyl chloride → (E)-2'-Deoxy-2'-(fluoromethylene)cytidine 5'-ethylenediphosphonate

https://huagongshe.com/reaction/1157351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1,2-Ethylenediphosphonic AcidHCID 80247—
ReactantTezacitabineHCID 6435808—
SolventDimethylformamideHCID 6228—
Product(E)-2'-Deoxy-2'-(fluoromethylene)cytidine 5'-ethylenediphosphonateHCID 865915142.7%

Reaction Steps

Ethylenediphosphonic acid (100 mg, 0.53 mmol) was treated with oxalyl chloride (2 mL, as solvent) and anhydrous DMF (0.1 mL, cat.). After heating at reflux for 10 minutes under an argon atmosphere a solution was obtained and after a further 3 h the reaction mixture was cooled to room temperature and concentrated in vacuo. The residue was coevaporated with anhydrous acetonitrile (3×10 mL). The residue was dissolved in anhydrous trimethyl phosphate (2 mL), cooled to −15° C. under an argon and (E)-2′-deoxy-2′-(fluoromethylene)cytidine (64 mg, 0.25 mmol) was added. After stirring for 2 h the reaction mixture was quenched with ice-cold TEAB solution (1.0 M, 5 mL) and stirred for 30 minutes. Purification by HPLC gave 2.9 mg of the titled compound 80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807653B2
Source datasetuspto-grants-2010_10
ORD IDord-1d773c1d2be2451486d5fe319b1e20ef
Source noteuspto-grants-2010_10