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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657080Generated: October 30, 2026

Allyl iodide → HCID 68816871, compound

https://huagongshe.com/reaction/657080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantPotassium CarbonateHCID 11430—
Reactant7-fluoro-1,5-naphthyridin-2(1H)-one 5-oxideHCID 68816493—
SolventDimethylformamideHCID 6228—
ProductHCID 68816871HCID 68816871—

Reaction Steps

Crude 7-fluoro-1,5-naphthyridin-2(1H)-one 5-oxide (0.995 g, 5.524 mmol) and potassium carbonate were stirred in anhydrous DMF (20 mL) under argon, and allyl iodide (1.5 mL, ca. 3 eq.) was added. The mixture was stirred at rt overnight. The solvent was removed under reduced pressure and the residue was partitioned between DCM (100 mL) and water (50 mL). The organic phase was separated using a hydrophobic frit and the aqueous phase was extracted with DCM (2×50 mL). The combined organic extracts were dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure to give the crude product as a brown gum. This was purified by column chromatography on silica gel eluted with 0-10% methanol in DCM. Appropriate fractions were combined and evaporated under reduced pressure to give 7-fluoro-1-(2-propen-1-yl)-1,5-naphthyridin-2(1H)-one 5-oxide (0.341 g) as a tan amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-cc1ad70fedf34e5c8a48f2bfc63117f2
Source noteuspto-grants-2011_12