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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213083Generated: October 30, 2026

Sodium Carbonate → HCID 21956061, compound

https://huagongshe.com/reaction/2213083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluorophenylboronic acidHCID 2734354—
Reactant6-Bromo-3-nitro-2-pyridinamineHCID 12097745—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 21956061HCID 21956061100%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of 6-amino-2-bromo-5-nitropyridine (2.0 g, 9.2 mmol) and 2-fluorophenylboronic acid (2.57 g, 18 mmol) in dimethoxyethane (60 mL) were added 2M aqueous sodium carbonate solution (18 mL) and tetrakistriphenylphosphine palladium(0) (106 mg, 0.092 mmol). The mixture was stirred at 105° C. for 16 hours under a nitrogen atmosphere. After the reaction mixture was cooled to room temperature, it was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was dissolved in a mixture of ethyl acetate (30 mL) and methanol (30 mL). To the solution was added 10% palladium carbon (200 mg), and the mixture was stirred at room temperature for 14 hours under a hydrogen atmosphere. After removal of the palladium catalyst by filtration, the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (chloroform:methanol=30:1) to give the title compound (1.87 g, 100%) as a reddish brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105526B2
Source datasetuspto-grants-2006_09
ORD IDord-affd993f060340d5ae2e64d5427f597d
Source noteuspto-grants-2006_09