HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074340Generated: October 30, 2026
Sodium Carbonate → Tert-butyl 4-{2-[1-(6-methylpyridin-2-yl)piperidin-4-yl]ethyl}piperidine-1-carboxylate
https://huagongshe.com/reaction/2074340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-Chloro-2-picoline | HCID 87601 | — |
| Reactant | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | Tert-butyl 4-[2-(piperidin-4-yl)ethyl]piperidine-1-carboxylate hydrochloride | HCID 57421848 | — |
| Catalyst | (1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladium | HCID 15673654 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4-{2-[1-(6-methylpyridin-2-yl)piperidin-4-yl]ethyl}piperidine-1-carboxylate | HCID 57507817 | 50.4% |
Reaction Steps
2-(Dicyclohexylphosphino)biphenyl (71 mg) and (1E,4E)-1,5-diphenyl-1,4-pentadien-3-one-palladium (93 mg) were added to a toluene (10 ml) suspension of tert-butyl 4-(2-piperidin-4-ylethyl)piperidine-1-carboxylate hydrochloride (1.13 g), 2-chloro-6-methylpyridine (431 mg) and sodium tert-butoxide (487 mg), followed by stirring at 120° C. for 1 hour. The reaction liquid was left cooled, then an aqueous saturated sodium carbonate solution was added thereto, followed by extraction with EtOAc. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated and the residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=10:1 (v/v)) to obtain tert-butyl 4-{2-[1-(6-methylpyridin-2-yl)piperidin-4-yl]ethyl}piperidine-1-carboxylate (660 mg) as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919495B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-48ffc657188f424b84d45be16d14c2ef |
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| Source note | uspto-grants-2011_04 |
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