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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920691Generated: October 30, 2026

2'-Deoxy-2'-fluoro-2'-methyluridine → HCID 45102209, compound

https://huagongshe.com/reaction/1920691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-Deoxy-2'-fluoro-2'-methyluridineHCID 11311503—
ReactantHCID 131729699HCID 131729699—
ReactantHCID 178418441HCID 178418441—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 45102209HCID 45102209—

Reaction Steps

To a stirred solution of 1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione (730 mg, 2.8 mmol) in dry pyridine (15 mL) was added a 0.45M solution of tetrazole in acetonitrile (15 mL) followed by bis(N,N-diisopropylamino)methylphosphite (0.971 mL, 3.3 mmol) at room temperature. After 2 h, TLC indicated disappearance of the starting material and two non-polar products. The reaction mixture was concentrated under reduced pressure at room temperature and the residue was triturated with EtOAc (30 mL). Tetrazole salts precipitated were filtered off and the filtrate was concentrated under reduced pressure. The residue was chromatographed using 0-40% EtOAc/hexanes gradient to give pure product 2 (92 mg) and mixture of product 1&2 (102 mg). 1H NMR confirmed that the product 2 is a single isomer of the required compound. Stereochemistry is not determined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173621B2
Source datasetuspto-grants-2012_05
ORD IDord-a11a138ffd5445958ccbda82a7eeb51c
Source noteuspto-grants-2012_05