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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161923Generated: October 29, 2026

Acetic Acid → HCID 23626787, compound

https://huagongshe.com/reaction/1161923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfateHCID 6497—
ReactantLithium hydrideHCID 62714—
ReactantHCID 178499097HCID 178499097—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23626787HCID 23626787—

Reaction Conditions

Temperature38 °C

Reaction Steps

Methyl-5-(benzoyloxy)-2-{(2S,4S)-1-[(benzyloxy)carbonyl]-4-fluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate, dissolved in dry dioxane, was added to a suspension of lithium hydride (1.2 eq.) in dry dioxane. The reaction mixture was stirred at 38° C. for 45 minutes and then cooled down to room temperature. Dimethyl sulfate (1.3 eq.) was added and the mixture was heated to 58° C. and stirred at this temperature for 3 hours. The reaction mixture was then cooled down and glacial acetic acid (0.2 eq.) was added, followed by water and ethyl acetate. The aqueous layer was separated and extracted with ethyl acetate; the organic phase was dried over Na2SO4 and filtered to give, after concentration, a crude that was purified by flash chromatography (eluent petroleum ether: ethyl acetate from 4:6 to 2:8) to give the title compound as a 4.6:5.4 mixture of rotamers by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820660B2
Source datasetuspto-grants-2010_10
ORD IDord-f26f3ce993aa43cb9fd253a470b160be
Source noteuspto-grants-2010_10