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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41295Generated: October 28, 2026

2-Bromopyridine → [2,3'-Bipyridine]-6'-carboxylic acid

https://huagongshe.com/reaction/41295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant2-Methoxycarbonyl-5-pyridineboronic acid, pinacol esterHCID 46738663—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product[2,3'-Bipyridine]-6'-carboxylic acidHCID 5735885323.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 5 ml microwave vial were added 2-bromopyridine (0.093 ml, 0.949 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinecarboxylate (300 mg, 1.139 mmol), bis(triphenylphosphine)palladium(II) chloride (133 mg, 0.190 mmol), sodium carbonate (302 mg, 2.85 mmol), 1,2-dimethoxyethane (1.5 ml), ethanol (1.000 ml) and water (0.500 ml). The reaction mixture was heated for 0.5 hours at 120° C. in the microwave. The mixture was diluted with MeOH and filtered through Celite®. The product was concentrated in vacuo then filtered through a 20 g SCX cartridge (washed with MeOH, eluted with 1M NH3 in MeOH) and evaporated in vacuo. The product was triturated with ether and concentrated under vacuo. The product was diluted in DCM then 1 ml of 1M HCl in ether added and the product was concentrated in vacuo then was dissolved in MeCN/DMSO 1:1 and purified by MDAP. The desired fractions were collected and concentrated under vacuo to give the title compound (44 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530478B2
Source datasetuspto-grants-2013_09
ORD IDord-9ecab71c57fd40988bfeff16b7449608
Source noteuspto-grants-2013_09