HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355579Generated: November 2, 2026
N-Benzoyl-4-piperidone → HCID 178479671, compound
https://huagongshe.com/reaction/1355579
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Benzoyl-4-piperidone | HCID 90583 | — |
| Reactant | HCID 178479294 | HCID 178479294 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178479671 | HCID 178479671 | 86.4% |
Reaction Steps
To a solution of (1R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-imidazol-2-yl)-1-ethanamine hydrochloride (1 g, 2.65 mmol) in isopropanol (15 ml) was added N-benzoyl-4-piperidone (2.64 g, 13 mmol). The solution was refluxed for about one hour and cooled to about 20° C. The solvent was removed under reduced pressure. The residue was treated with dichloromethane (30 ml) and stirred for about 30 min at about 20° C. The resulting precipitate was collected by filtration, washed with dichloromethane and diethyl ether, and dried to afford 1.2 g of the title product as the hydrochloride salt. Melting point: 240-244° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586445B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-3e0ff5be7cd149cfbd204c6d7dd67b14 |
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| Source note | uspto-grants-2003_07 |
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