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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534950Generated: October 30, 2026

Triethylamine → 5-{2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoethyl}imidazolidine-2,4-dione

https://huagongshe.com/reaction/534950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHydantoin-5-acetic acidHCID 95492—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
SolventDimethylformamideHCID 6228—
Product5-{2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoethyl}imidazolidine-2,4-dioneHCID 6675103570.1%

Reaction Steps

A suspension of 1-(2-tert-butylphenyl)piperazine dihydrochloride (Reference Example 1, 0.400 g, 1.37 mmol), (2,5-dioxoimidazolidin-4-yl)acetic acid (0.261 g, 1.65 mmol), EDCI (0.311 g, 1.65 mmol), HOBt (0.223 g, 1.65 mmol) and triethylamine (496 μl, 3.56 mmol) in DMF (13 mL) was stirred at room temperature for 16 h. The reaction mixture was poured into saturated ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with saturated sodium hydrogen carbonate solution and brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to give crude product. The product was purified by re-crystallization from THF and n-hexane to provide 5-{2-[4-(2-tert-butylphenyl)piperazin-1-yl]-2-oxoethyl}imidazolidine-2,4-dione (0.344 g, 70%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-8508b38d5eba41a78166e67ef91be6d5
Source noteuspto-grants-2014_10