HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699264Generated: October 30, 2026
1-(4-Pyridyl)piperazine → HCID 54052804, compound
https://huagongshe.com/reaction/1699264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Boc-Lys(Z)-OH | HCID 2724765 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54052804 | HCID 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 overnight 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344449B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-68d67093d9804ada9296524a44f0d543 |
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| Source note | uspto-grants-2002_02 |
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