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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667377Generated: November 1, 2026

Sodium Iodide → HCID 24798259, compound

https://huagongshe.com/reaction/1667377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-cyclopentyl 2-amino-4-methylpentanoateHCID 53718217—
ReactantHCID 57658448HCID 57658448—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 24798259HCID 2479825952%

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 (138 mg, 0.29 mmol) in anhydrous DMF (3 ml) under an atmosphere of nitrogen was added cyclopentyl L-leucinate (Intermediate 8) (284 mg, 1.43 mmol, 5 eq), sodium iodide (86 mg, 0.57 mmol, 2 eq) and N,N-diisopropylethylamine (0.052 ml, 0.29 mmol, 1 eq). The mixture was heated at 90° C. for 16 hours, before being allowed to cool to room temperature and diluted with EtOAc (25 ml). The solution was washed with water (2×25 ml) and brine (25 ml). The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. Purification by column chromatography (3-4% MeOH in DCM) followed by preparative HPLC afforded the title compound as a cream coloured solid (96 mg, 52% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044211B2
Source datasetuspto-grants-2011_10
ORD IDord-47f5de055aca467081eb92f6d2fb5848
Source noteuspto-grants-2011_10