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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347686Generated: November 1, 2026

Sodium Carbonate → 5'-Bromo-2'-chloro-2-methyl-[3,4']bipyridinyl

https://huagongshe.com/reaction/347686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant2-Methylpyridin-3-yl trifluoromethanesulfonateHCID 10776465—
Reactant5-Bromo-2-chloro-4-iodopyridineHCID 21865140—
CatalystCID 53485975HCID 53485975—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5'-Bromo-2'-chloro-2-methyl-[3,4']bipyridinylHCID 21083636—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.73 g (11.3 mmol) trifluoro-methanesulfonic acid 2-methyl-pyridin-3-yl ester, 3.16 g (12.4 mmol) bis(pinacolato)diboron, 3.33 g (33.9 mmol) potassium acetate and 0.46 g (0.56 mmol) dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct in 75 ml N,N-dimethylformamide was heated at 80° C. over night under argon. After cooling to room temperature 5.40 g (17.0 mmol) 5-bromo-2-chloro-4-iodo-pyridine, another portion of 0.46 g (0.56 mmol) dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct and 30 ml of a deoxygenated 2 M aqueous solution of sodium carbonate were added. The reaction mixture was heated at 80° C. for 4.5 h. After cooling to room temperature the mixture was diluted with water and extracted with three portions of tert-butyl methyl ether. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. Flash column chromatography gave 1.00 (31%) of the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176205B2
Source datasetuspto-grants-2007_02
ORD IDord-f81d9b9275dd4c88bebb38278d438da4
Source noteuspto-grants-2007_02