HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932543Generated: November 4, 2026
1-Benzylpiperazine → HCID 68525626, compound
https://huagongshe.com/reaction/1932543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 68525974 | HCID 68525974 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68525626 | HCID 68525626 | — |
Reaction Steps
To a solution of 1-{4-[5-(3,4-dichlorobenzoylamino)pyridin-2-yloxy]benzoyl}piperidine-4-carboxylic acid (4.5 g, 8.8 mmol) in DMF (88 mL) were added 1-benzylpiperazine (1.83 mL, 10.5 mmol), 1-hydroxybenzotriazole monohydrate (1.61 g, 10.5 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.02 g, 10.5 mmol) under ice cooling, and the resulting solution was stirred overnight at room temperature. To this reaction solution was added a saturated sodium bicarbonate solution, and the resulting solution was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was recrystallized from isopropyl alcohol (700 mL), to thereby yield 3.2 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188277B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-3a8ada9762fe400a8d5ab85299b23ab2 |
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| Source note | uspto-grants-2012_05 |
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