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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605796Generated: October 31, 2026

6-Chloro-2-picoline → HCID 57507761, compound

https://huagongshe.com/reaction/605796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-2-picolineHCID 87601—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 57421831HCID 57421831—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
ProductHCID 57507761HCID 5750776191.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

In an argon atmosphere, sodium tert-butoxide, (0.52 g), tris(dibenzylideneacetone)dipalladium (100 mg) and 2-(dicyclohexylphosphino)biphenyl (76 mg) were added to a Tol (22 ml) solution of 2-chloro-6-methylpyridine (0.56 g) and tert-butyl 4-[3-(4-piperidinyl)propyl]-1-piperidinecarboxylate (1.1 g), followed by heating with stirring at 100° C. for 1 hour. This was cooled to room temperature, diluted with EtOAc, and washed with aqueous saturated sodium hydrogencarbonate solution. This was dried over anhydrous magnesium sulfate, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=10:1 (v/v)) to obtain tert-butyl 4-{3-[1-(6-methyl-2-pyridinyl)-4-piperidyl]propyl}-1-piperidinecarboxylate (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915261B2
Source datasetuspto-grants-2011_03
ORD IDord-457187bb4e8a423a855019c5f187b403
Source noteuspto-grants-2011_03