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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant6-Chloro-2-picolineHCID 87601—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
ReactantSodium t-butoxideHCID 23676156—
ReactantTert-butyl 4-[2-(piperidin-4-yl)ethyl]piperidine-1-carboxylate hydrochlorideHCID 57421848—
Catalyst(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladiumHCID 15673654—
SolventTolueneHCID 1140—
ProductTert-butyl 4-{2-[1-(6-methylpyridin-2-yl)piperidin-4-yl]ethyl}piperidine-1-carboxylateHCID 5750781750.4%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919495B2
Source datasetuspto-grants-2011_04
ORD IDord-48ffc657188f424b84d45be16d14c2ef
Source noteuspto-grants-2011_04