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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157352Generated: October 25, 2026

Gemcitabine → 2'-Deoxy-2',2'-difluorocytidine 5'-ethylenediphosphonate

https://huagongshe.com/reaction/1157352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGemcitabineHCID 60750—
ReactantOxalyl chlorideHCID 65578—
Reactant1,2-Ethylenediphosphonic AcidHCID 80247—
SolventDimethylformamideHCID 6228—
Product2'-Deoxy-2',2'-difluorocytidine 5'-ethylenediphosphonateHCID 497680393.9%

Reaction Steps

Ethylenediphosphonic acid (173 mg, 0.91 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 argon, a solution was obtained and after a further 3 h the reaction mixture was cooled to room temperature and evacuated in vacuo. The residue was co-evaporated with anhydrous acetonitrile (3×10 ml). The residue was dissolved in anhydrous trimethyl phosphate (2 mL), cooled to −15° C. and 2′deoxy-2′,2′-difluorocytidine (93 mg, 0.46 mmol) was added under argon. 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 7.8 mg of the titled compound 81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807653B2
Source datasetuspto-grants-2010_10
ORD IDord-878d714863ef449a92d58a60a3ff4825
Source noteuspto-grants-2010_10