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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667378Generated: October 30, 2026

Sodium Iodide → HCID 57658405, compound

https://huagongshe.com/reaction/1667378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl (2S)-2-amino-4-methylpentanoate hydrochlorideHCID 12451443—
ReactantHCID 57658448HCID 57658448—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57658405HCID 5765840518%

Reaction Conditions

Temperature90 °C

Reaction Steps

From Intermediate 4G. To a solution of 6-Amino-1-{4-[(5-chloropentyl)oxy]-2,6-difluorophenyl}-5-(2,4-difluorobenzoyl)pyridin-2(1H)-one (96 mg, 0.20 mmol) in anhydrous DMF (3 ml) under an atmosphere of nitrogen was added tert-butyl L-leucinate hydrochloride (198 mg, 0.99 mmol, 5 eq), sodium iodide (60 mg, 0.40 mmol, 2 eq) and N,N-diisopropylethylamine (0.072 ml, 0.40 mmol, 2 eq). The mixture was heated at 90° C. for 20 hours, before being allowed to cool to room temperature and diluted with EtOAc (20 ml). The solution was washed with water (2×20 ml) and brine (20 ml). The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. Purification by column chromatography (1-3% MeOH in DCM) followed by preparative HPLC afforded the title compound as a white solid (23 mg, 18% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044211B2
Source datasetuspto-grants-2011_10
ORD IDord-2149f8f6ab9949cc896afa7351dc8476
Source noteuspto-grants-2011_10