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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592184Generated: October 30, 2026

Dimethylformamide → Diethyl 2-(2',3-dimethyl-2,4'-bipyridin-5-yl)malonate

https://huagongshe.com/reaction/592184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium FluorideHCID 522689—
Reactant2-Methyl-4-(tributylstannyl)pyridineHCID 21660574—
ReactantDiethyl 2-(6-chloro-5-methylpyridin-3-yl)malonateHCID 58447937—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 2-(2',3-dimethyl-2,4'-bipyridin-5-yl)malonateHCID 58447640—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a reaction flask containing diethyl 2-(6-chloro-5-methylpyridin-3-yl)malonate 156-3 (1.00 g, 4.00 mmol), 2-methyl-4-(tributylstannyl)pyridine (1.53 g, 4.00 mmol) and Pd(PPh3)4 (440 mg, 0.4 mmol) under argon was added DMF (20 mL). The mixture was stirred at 120° C. for 10 hours. After the mixture was cooled down to room temperature, 1N KF aqueous solution was added to it and stirred for 15 minutes. The mixture was diluted with ethyl acetate and the two layers were separated. The organic layer was further washed with water and brine, dried over Na2SO4, concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol in dichloromethane to give diethyl 2-(2′,3-dimethyl-2,4′-bipyridin-5-yl)malonate 156-4 as colorless oil. MS m/z 343.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238646B2
Source datasetuspto-grants-2016_01
ORD IDord-691b6da43a8b481bb483f63b36ecb242
Source noteuspto-grants-2016_01