HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190145Generated: October 31, 2026
Triethylamine → 4-{[4,5-Bis(3-chlorophenyl)furan-2-yl]carbonyl}piperazin-2-one
https://huagongshe.com/reaction/2190145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | 4,5-Bis(3-chlorophenyl)furan-2-carboxylic acid | HCID 58064763 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-{[4,5-Bis(3-chlorophenyl)furan-2-yl]carbonyl}piperazin-2-one | HCID 58064791 | — |
Reaction Steps
600 mg (1.07 mmol) of the compound from Example 25A are provided in 14 ml of dry toluene, 0.24 ml (3.22 mmol) of thionyl chloride are added and the mixture is heated under reflux for 2.5 hours. The reaction mixture is concentrated, and the residue is taken up in 10 ml of dichloromethane and cooled to 0° C. 0.24 ml (1.72 mmol) of triethylamine and then 172 mg (1.72 mmol) of piperazin-2-one are then added, and the reaction mixture is stirred at RT overnight. The mixture is subsequently concentrated and the residue is purified by preparative HPLC (RP18 column; eluent: acetonitrile/water gradient). 302 mg (68% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324268B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a7ce85e68c684580bc85b092a83f9487 |
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| Source note | uspto-grants-2012_12 |
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