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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235Generated: October 28, 2026

1-(4-Pyridyl)piperazine → HCID 18918452, compound

https://huagongshe.com/reaction/2235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Pyridyl)piperazineHCID 70517—
ReactantHCID 18918336HCID 18918336—
SolventAcetonitrileHCID 6342—
ProductHCID 18918452HCID 18918452—

Reaction Conditions

Temperature30 °C

Reaction Steps

1-(4-Pyridyl)piperazine (1.63 g) was dissolved in warm acetonitrile (25 ml), the solution cooled to 30° C. and with stirring, a solution of methyl 4-(4-bromomethylphenyl)butyrate in acetonitrile (5 ml) added. After 30 minutes the resulting precipitate was removed by filtration and the filtrate concentrated in vacuo to give a yellow oil. Purification by flash chromatography on silica, eluting with 0 to 4% v/v methanol/dichloromethane gave a solid. Trituration with ether and removal of the insoluble solid gave a clear solution. Concentration of this solution gave the title compound, 0.90 g, as a white fluffy solid: m.p. 126°-127° C.; NMR (d6DMSO) δ 8.14 (2H, d), 7.24 (2H, d), 7.14 (2H, d), 6.77 (2H, d), 3.59 (3H, s), 3.48 (2H, s), 3.30 (4H, t), 2.59 (2H, t), 2.47 (4H, t), 2.32 (2H, t), 1.63 (2H, m); m/e 354 (M+H)+ ; calculated for C21H27N3O2.0.25H2O: C, 70.4; H, 7.7; N, 11.7. found: C, 70.6; H, 7.6; N, 11.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728701
Source datasetuspto-grants-1998_03
ORD IDord-8cd1790f4528490e93ace90911d115bc
Source noteuspto-grants-1998_03