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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782724Generated: October 31, 2026

1-(4-Pyridyl)piperazine → HCID 54052804, compound

https://huagongshe.com/reaction/1782724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Pyridyl)piperazineHCID 70517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantBoc-Lys(Z)-OHHCID 2724765—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventDimethylformamideHCID 6228—
ProductHCID 54052804HCID 54052804—

Reaction Steps

To a mixture of 18.8 g (0.0494 mol) of Boc-Lys(Z)-OH, 6.5 g (0.05 mol) of DIEA, 16 g (0.05 mol) of TBTU, 6.6 g (0.049 mol) of HOBt and 100 ml of dimethylformamide were added dropwise, with stirring, 8.1 g (0.0494 mol) of 1-(4-pyridinyl)piperazine, dissolved in 40 ml of DMF, and the mixture was stirred over-night at room temperature. The solvent was removed in vacuo and the residue was taken up in ethyl acetate. The ethyl acetate phase was then washed three times successively with 70 ml of saturated aqueous sodium hydrogen carbonate solution and once with 70 ml of saturated aqueous saline solution, dried over sodium sulphate and evaporated down in vacuo. 24.2 g (93.2% of theory) of a yellowish oil were obtained, which was used for the following reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498325B2
Source datasetuspto-grants-2009_03
ORD IDord-5eacc857d6964c20a82176fc7227bf45
Source noteuspto-grants-2009_03