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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667363Generated: November 2, 2026

Sodium Iodide → HCID 57658448, compound

https://huagongshe.com/reaction/1667363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-5-chloropentaneHCID 96070—
ReactantHCID 58608543HCID 58608543—
ReactantHCID 67444810HCID 67444810—
SolventAcetoneHCID 180—
ProductHCID 57658448HCID 57658448—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 6-amino-5-(2,4-difluorobenzoyl)-1-(2,6-difluoro-4-hydroxyphenyl)-pyridin-2(1H)-one (300 mg, 0.79 mmol) in acetone (6 ml) under an atmosphere of nitrogen was added 1-bromo-5-chloropentane (0.115 ml, 0.87 mmol, 1.1 eq), sodium iodide (238 mg, 1.59 mmol, 2 eq) and potassium carbonate (438 mg, 3.17 mmol, 4 eq). The mixture was heated at 70° C. for 16 hours, before being allowed to cool to room temperature and partitioned between EtOAc (50 ml) and water (50 ml). The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. Purification by column chromatography (30% EtOAc in heptane) afforded a 3:2 mixture of the title compound and 6-amino-1-{4-[(5-iodopentyl)oxy]-2,6-difluorophenyl}-5-(2,4-difluorobenzoyl)pyridin-2(1H)-one (142 mg) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044211B2
Source datasetuspto-grants-2011_10
ORD IDord-b327cb246d3f4045a608e75bf0fba842
Source noteuspto-grants-2011_10