HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371205Generated: October 31, 2026
HCID 13094812, compound → HCID 57656882, compound
https://huagongshe.com/reaction/2371205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13094812 | HCID 13094812 | — |
| Reactant | HCID 57656776 | HCID 57656776 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57656882 | HCID 57656882 | 62.2% |
Reaction Steps
A mixture of the alkenes N-(3,4-dichlorophenyl)-4-[1-ethylpiperidin-3-yl)methyl]-3,6-dihydropyridine-1(2H)-carboxamide and N-(3,4-dichlorophenyl)-4-[(1-ethylpiperidin-3-yl)methylene]piperidine-1-carboxamide (3:1) (40 mg) and 10% palladium on charcoal (30 mg) in ethanol (5 mL) was evacuated and purged with hydrogen. The mixture was left under an atmosphere of hydrogen for 4 hrs and then filtered through celite. The celite pad was washed with ethanol and the filtrate evaporated. The residue was purified using reverse phase HPLC eluting with a mixture of 5-95% acetonitrile in water and then by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in dichloromethane to give the title compound as a white solid (25 mg, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710224B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-460a87e19ef84665bc5a25cf0c181bc6 |
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| Source note | uspto-grants-2014_04 |
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