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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972689Generated: October 31, 2026

Potassium Carbonate → 5-((4-Bromo-3-methylphenyl)sulfonyl)-2-pyridinamine

https://huagongshe.com/reaction/1972689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant2-Pyridinamine, 5-iodo-HCID 88579—
ReactantSodium 4-bromo-3-methylbenzenesulfinateHCID 23712900—
CatalystCopper iodideHCID 83717—
SolventDimethyl SulfoxideHCID 679—
Product5-((4-Bromo-3-methylphenyl)sulfonyl)-2-pyridinamineHCID 6658255920.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium 4-bromo-3-methylbenzenesulfinate (2.92 mg, 11.36 mmol), 2-amino-5-iodopyridine (1.25 g, 5.68 mmol, Alfa Aesar, Ward Hill, Mass.), copper iodide (216 mg, 1.14 mmol, Strem Chemical Inc, Newburyport, Mass.), potassium carbonate (785 mg, 5.68 mmol), N,N-dimethylethylenediamine (0.25 mL, 2.27 mmol, Alfa Aesar, Ward Hill, Mass.), and DMSO (15 mL) were added to a reaction vial. The vial was closed, purged with nitrogen for several minutes, and heated at 100° C. for 16 h. After cooling to room temperature, the reaction mixture was diluted with water (20 mL) and extracted with EtOAc (20 mL×3). The combined organic extracts were dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude material. The crude material was absorbed onto a plug of silica gel and purified by chromatography through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 20% to 50% EtOAc in hexane, to provide 5-((4-bromo-3-methylphenyl)sulfonyl)-2-pyridinamine (377 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-40091d83c8fc4ca3b1e4fa00b22941d0
Source noteuspto-grants-2013_04