HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 66754327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 5-Oxo-pyrrolidine-3-carboxylic acid pentafluorophenyl ester | HCID 86640155 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66754327 | HCID 66754327 | 107% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119623B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-170a2140955e434da021048ded2acd6d |
| Source note | uspto-grants-2012_02 |