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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498252Generated: October 30, 2026

Potassium Carbonate → HCID 69487238, compound

https://huagongshe.com/reaction/498252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoisonicotinic acidHCID 222701—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
ReactantHCID 46317480HCID 46317480—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69487238HCID 69487238—

Reaction Conditions

Temperature80 °C

Reaction Steps

The title compound was prepared from [2,4′]bipyridinyl-4-carboxylic acid methyl ester [prepared by the following procedure: A mixture of pyridine-4-boronic acid (0.7 g, 5.7 mmol), 2-bromo-isonicotinic acid (1.15 g, 5.7 mmol) and K2CO3 (0.63 g, 4.6 mmol) in CH3CN (120 ml)/H2O (10 ml) was degassed and Pd(PPh3)4 (0.13 g, 0.11 mmol) was added. The mixture was stirred for 24 h at 80° C. in an atmosphere of nitrogen and then concentrated in vacuum to a volume of about 10 ml. The pH was set to 6 by addition of 3N HCl and the solution was then evaporated in vacuum to dryness. The residue was stirred in 1N HCl-MeOH (23 ml) for 65 h at 50° C. The crude product was purified by chromatography (silica gel, AcOEt/cyclohexane 1:1) to give the methyl ester as light yellow oil (0.37 g).] (0.21 g, 1.0 mmol) by treatment with lithium tert-butyl acetate according to general procedure K (method b). Obtained as a light yellow oil (0.45 g, crude product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949542B2
Source datasetuspto-grants-2005_09
ORD IDord-9b7cd606c66f4c9f9a3ef8eb3db82f98
Source noteuspto-grants-2005_09