Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291816Generated: October 31, 2026

1-(4-Pyridyl)piperazine → HCID 18918610, compound

https://huagongshe.com/reaction/1291816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Pyridyl)piperazineHCID 70517—
ReactantEthyl 1-(bromoacetyl)piperidine-4-carboxylateHCID 23368650—
SolventAcetonitrileHCID 6342—
ProductHCID 18918610HCID 1891861032.4%

Reaction Steps

A solution of ethyl-1-(bromoacetyl)-piperidin-4-carboxylate (0.84 g, 3 mMoles) in acetonitrile (10 ml) was added dropwise to a stirred solution of 1-(4-pyridyl)piperazine (0.5 g, 3 mMoles) in acetonitrile (20 ml) and the resulting mixture was allowed to stand for 3 hours. The white precipitate was removed by filtration and the mother liquors were concentrated under reduced pressure to give a yellow foam. The foam was purified by chromatography (flash column made with grade III neutral alumina and eluted with a gradient of 0-1% ethanol in dichloromethane) to give the title compound (350 mg) as a colourless oil which was crystallised from cyclohexane to give colourless prisms; mp 102°-104° C.; Microanalysis, found: C,63.5; H,8.1; N, 15.5%; C19H28N4O3 requires C,63.3; H,7.8; N,15.5%; NMR (d6DMSO+CD3COOD): 1.2 (t,3H), 1.3-1.7 (m,2H), 1.8 (m,2H), 2.5-2.8 (m,6H), 3.0-3.4 (m,3H), 3.6 (br s,4H), 3.9 (d,1H), 4.0 (q,2H), 4.2 (d,1H), 7.1 (d,2H), 8.2 (d,2H); m/e 361 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753659
Source datasetuspto-grants-1998_05
ORD IDord-7cda7a5650da46c0823122b620fb852c
Source noteuspto-grants-1998_05