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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685382Generated: October 30, 2026

Citric Acid → Ethyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxo-3-pyridin-2-ylimidazolidin-1-yl]acetate

https://huagongshe.com/reaction/1685382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantAnilineHCID 6115—
Reactant2-BromopyridineHCID 7973—
ReactantPotassium AcetateHCID 517044—
ReactantEthyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxoimidazolidin-1-yl]acetateHCID 91574597—
CatalystCopperHCID 23978—
CatalystCuprous chlorideHCID 62652—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductEthyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxo-3-pyridin-2-ylimidazolidin-1-yl]acetateHCID 123216751—

Reaction Steps

A stirred solution of ethyl[5-(3,5-difluorophenyl)-5-methyl-2,4-dioxoimidazolidin-1-yl]acetate, isomer A (100 mg, 0.320 mmol, described in Intermediate 7), 2-bromopyridine (0.156 mL, 1.60 mmol), copper powder (71.2 mg, 1.12 mmol), copper (I) chloride (6.34 mg, 0.064 mmol), and potassium acetate (94.0 mg, 0.961 mmol) in pyridine (1.8 mL) was heated at 100° C. for 18 h. The cooled reaction mixture was poured onto 10% citric acid (20 mL) and with EtOAc (3×20 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 50:50, to provide the title compound. MS: m/z=390 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148390B2
Source datasetuspto-grants-2012_04
ORD IDord-cfcf6faedb6b4c98a25f17fd6a0d0008
Source noteuspto-grants-2012_04