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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Hydantoin-5-acetic acid | HCID 95492 | — |
| Reactant | 1-(2-Tert-butylphenyl)piperazine dihydrochloride | HCID 66751149 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-{2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoethyl}imidazolidine-2,4-dione | HCID 66751035 | 70.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-8508b38d5eba41a78166e67ef91be6d5 |
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| Source note | uspto-grants-2014_10 |
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