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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930758Generated: October 28, 2026

Potassium Carbonate → HCID 53217788, compound

https://huagongshe.com/reaction/930758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Methylthio)phenylboronic acidHCID 2733959—
Reactant4-Bromo-2-methoxypyridineHCID 14062309—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 53217788HCID 5321778877.8%

Reaction Conditions

Temperature95 °C

Reaction Steps

A suspension of 4-bromo-2-methoxypyridine (1.225 g, 6.511 mmol), 4-methylthiophenyl boronic acid (2.188 g, 13.02 mmol), PdCl2(dppf) (531 mg, 0.651 mmol) and K2CO3 (1.797 g, 13.02 mmol) in DMSO (10 mL) was degassed under reduced pressure for 25 min. The suspension was put under N2 and stirred at 95° C. for 16 h. The suspension was cooled, H2O was added, and the suspension was filtered to afford a light colored solid. Flash chromatography (silica gel, hexanes/(1:1 EtOAc/hexanes), 100:0 to 0:100) afforded 1.10 g of a white powder. The white powder was diluted with concentrated HCl solution (50 mL) and stirred at reflux for 24 h. The reaction was cooled and concentrated under reduced pressure. The residue was neutralized with saturated NaHCO3 solution, and the solid was collected by filtration. The solid was washed with H2O to afford the title compound (1.103 g, 71%) as a tan solid: 1H NMR (300 MHz, DMSO-d6) δ 7.65 (d, J=8.4 Hz, 2H), 7.43 (d, J=6.9 Hz, 1H), 7.34 (d, J=8.4 Hz, 2H), 6.57 (d, J=1.7 Hz, 1H), 6.50 (dd, J=6.9, 1.7 Hz, 1H), 3.34 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296743B2
Source datasetuspto-grants-2016_03
ORD IDord-1c505dace87e4ba698d867737df62f35
Source noteuspto-grants-2016_03