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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094791Generated: October 31, 2026

Potassium Carbonate → 3-(2,3-Dichlorophenyl)pyridine-2,6-diamine

https://huagongshe.com/reaction/1094791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromopyridine-2,6-diamineHCID 1415868—
Reactant2,3-Dichlorobenzeneboronic acidHCID 2734661—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(2,3-Dichlorophenyl)pyridine-2,6-diamineHCID 5758235735.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 3-bromopyridine-2,6-diamine (0.376 g, 2.00 mmol) in 1,4-dioxane (12 ml) and water (6 ml) was added 2,3-dichlorophenyl boronic acid (0.573 g, 3.00 mmol), potassium carbonate (0.552 g, 4.00 mmol) and palladium tetrakis(triphenylphosphine) (0.115 g, 0.01 mmol). The reaction was purged with nitrogen and heated at 80° C. for 18 hours. Further palladium tetrakis(triphenylphosphine) (0.115 g, 0.01 mmol) and 2,3-dichlorophenyl boronic acid (0.573 g, 3.00 mmol) were added and the reaction heated at 80° C. for a further 18 hours before concentrating in vacuo. The residue was taken up in ethyl acetate (20 ml) and washed with a saturated aqueous solution of K2CO3 before drying over MgSO4 and concentrating in vacuo. The residue was purified by silica gel column chromatography, eluting with 99:1 dichloromethane:methanol, then recrystallised from toluene to afford the title compound (0.180 g, 35% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-5942b936a5a347159b26a14ee07cd957
Source noteuspto-grants-2012_03