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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775361Generated: November 2, 2026

Piperazine → HCID 20785294, compound

https://huagongshe.com/reaction/1775361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-(2-Chloropyridin-4-yl)ethan-1-oneHCID 13145255—
SolventPyridineHCID 1049—
ProductHCID 20785294HCID 2078529421%

Reaction Steps

1-(2-Chloro-4-pyridyl)ethanone (156 mg, 1 mmol), piperazine (861 mg, 10 mmol) and pyridine (5 ml) were placed in a Radley vial and heated at reflux overnight. The mixture was concentrated under reduced pressure to dryness, the residue was mixed with toluene and evaporated under reduced pressure to remove excess of piperazine. The last step was repeated several times. The residue was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 51 mg of a solid (0.21 mmol, yield 21%) MS (multi-mode) m/z=206.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-bd85cb7d8612487385833b7ff2570745
Source noteuspto-grants-2016_02