HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885874Generated: October 31, 2026
1-Benzylpiperazine → HCID 24756555, compound
https://huagongshe.com/reaction/885874
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | HCID 59312563 | HCID 59312563 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 24756555 | HCID 24756555 | 31.5% |
Reaction Steps
1-Benzyl-piperazine (40 mg, 0.22 mmol) was added to a stirred mixture of methanesulfonic acid 4-((E)-3-{4-[(E)-2-(tetrahydro-pyran-2-yloxycarbamoyl)-vinyl]-phenyl}-acryloyl)-benzyl ester (prepared as described in Preparation 5, 90 mg, 0.185 mmol) and TEA (0.052 ml, 0.37 mmol) in DMF (2 ml). The resulting solution was stirred at room temperature for 1 h. The mixture was diluted with water and extracted with hot AcOEt. The organic phase was washed with water, dried over Na2SO4 and evaporated in vacuo. The crude reaction mixture was triturated with di-isopropylether/DCM, filtered and the resulting powder was suspended in DCM and treated with HCl/Et2O for 1 h. The solid was filtered and washed with DCM to give 28.1 mg of (E)-3-(4-{(E)-3-[4-(4-benzyl-piperazin-1-ylmethyl)-phenyl]-3-oxo-propenyl}-phenyl)-N-hydroxy-acrylamide as its bis-hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242175B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-8823ce4485714cfb9cfbd6dc27ea74d4 |
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| Source note | uspto-grants-2012_08 |
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