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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642046Generated: October 30, 2026

Piperazine → HCID 66754327, compound

https://huagongshe.com/reaction/1642046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDichloromethaneHCID 6344—
Reactant5-Oxo-pyrrolidine-3-carboxylic acid pentafluorophenyl esterHCID 86640155—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66754327HCID 66754327107%

Reaction Steps

To a suspension of 5-oxo-pyrrolidine-3-carboxylic acid pentafluorophenyl ester 17 (40.1 mg, 0.0578 mmol) in 2 mL THF extra dry was added piperazine (19.9 mg, 0.231 mmol) at room temperature. The reaction mixture was stirred for 10 hours at room temperature. Afterwards, 20 mL methylene chloride were added. The resulting organic layer was washed with 20 mL of a saturated aqueous solution of sodium hydrogenocarbonate, dried over magnesium sulfate and the solvent was removed in vacuo. Finally, the crude product was purified by chromatography on silica gel (ethyl acetate:methanol 9:1→1:1) to afford the desired 4-(piperazine-1-carbonyl)-pyrrolidin-2-one 18 as a white solid (12.2 mg, 45.91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119623B2
Source datasetuspto-grants-2012_02
ORD IDord-170a2140955e434da021048ded2acd6d
Source noteuspto-grants-2012_02