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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186762Generated: November 3, 2026

Dicyclohexylcarbodiimide → 2,5-Dioxopyrrolidin-1-yl 2-(2-fluoro-4-iodophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1186762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant2-(2-Fluoro-4-iodophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acidHCID 44189219—
Solvent1,4-DioxaneHCID 31275—
Product2,5-Dioxopyrrolidin-1-yl 2-(2-fluoro-4-iodophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 8666450485%

Reaction Steps

A 250 ml round-bottom flask was charged with 2-(2-fluoro-4-iodophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (2.0 g, 5.00 mmol) and dioxane (100 mL). To the resulting suspension was added 1-hydroxypyrrolidine-2,5-dione (0.63 g, 5.5 mmol) and DCC (0.63 g, 5.5 mmol). The reaction mixture was stirred at room temperature for 16 hours and filtered. The residue was concentrated under reduced pressure and purified by flash chromatography (Biotage system) using a gradient of EtOAc (0-50%) in hexane to afford the title product (2.1 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673919B2
Source datasetuspto-grants-2014_03
ORD IDord-611ae8c4b43c4694beb6615e0e1f7a00
Source noteuspto-grants-2014_03