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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829171Generated: November 2, 2026

Potassium Carbonate → (5S)-5-(3,4-Dichlorophenyl)-5-(1,3-dioxolan-2-yl methyl)-1-(6-methyl-2-pyridinyl)-2-piperidinone

https://huagongshe.com/reaction/1829171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-6-methylpyridineHCID 79205—
Reactant(5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinoneHCID 10882069—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(5S)-5-(3,4-Dichlorophenyl)-5-(1,3-dioxolan-2-yl methyl)-1-(6-methyl-2-pyridinyl)-2-piperidinoneHCID 58649121—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of (5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinone (WO 9807722) (6.5 g, 19.7 mmol), potassium carbonate (3.05 g, 21.7 mmol), copper (I) iodide (400 mg, 2.1 mmol) and 2-bromo-6-methylpyridine (10.2 g, 60 mmol) in 1-methyl-2-pyrrolidinone (200 ml) was stirred at 140° C. for 24 hours. The cooled mixture was partitioned between ethyl acetate and 10% aqueous ammonia, and the layers separated. The aqueous phase was extracted with ethyl acetate, and the combined organic extracts were washed with water, then brine (3×), dried (MgSO4) and evaporated under reduced pressure to give a gum. The crude product was purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (0:100 to 100:0) to afford the title compound as a brown solid, 3.02 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060836B2
Source datasetuspto-grants-2006_06
ORD IDord-50fe384090094a2e9bd3aa3d42777825
Source noteuspto-grants-2006_06