HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884193Generated: October 31, 2026
1-Piperonylpiperazine → HCID 68528799, compound
https://huagongshe.com/reaction/884193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Piperonylpiperazine | HCID 94426 | — |
| 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 68528799 | HCID 68528799 | — |
Reaction Steps
To a solution of 1-{4-[5-(3,4-dichlorobenzoylamino)pyridin-2-yloxy]benzoyl}piperidine-4-carboxylic acid (7.96 g, 15.5 mmol) in DMF (160 mL) were added 1-piperonylpiperazine (3.75 g, 17.6 mmol), 1-hydroxybenzotriazole monohydrate (2.85 g, 18.6 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (3.56 g, 18.6 mmol) under ice cooling, and the resulting solution was stirred for overnight at room temperature. This reaction solution was concentrated under reduced pressure. To the residue were added water and ethyl acetate, and the resulting solution was vigorously stirred. The resulting precipitates were collected by filtration and recrystallized from a dichloromethane-methanol mixed solvent, to thereby yield 7.36 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236826B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-7652e7b6bfd64d70943b3da4d60d7144 |
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| Source note | uspto-grants-2012_08 |
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