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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532501Generated: October 25, 2026

2-Furancarboxylic acid → Furan-2-carboxylic acid pyridazin-4-ylamide

https://huagongshe.com/reaction/532501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarboxylic acidHCID 6919—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant4-AminopyridazineHCID 298492—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductFuran-2-carboxylic acid pyridazin-4-ylamideHCID 5346668556.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.00 g (17.8 mmol) of furan-2-carboxylic acid were suspended in 25 mL of toluene and one drop of dimethylformamide was added to the mixture. 1.95 ml of thionylchloride (26.8 mmol) were added at room temperature and the reaction mixture was stirred at 80° C. for two hours. After removal of the solvent, toluene was added and the evaporation was repeated. The obtained residue was then dissolved in 5 ml of dichloromethane and the solution was added dropwise to a solution containing 1.70 g of pyridazin-4-yl-amine (17.8 mmol) and 2.73 ml of triethyl amine (19.6 mmol) in 20 ml of dichloromethane. The mixture was stirred at room temperature for 2 days and washed twice with water. The organic layer was dried over Na2SO4, filtered and the solvent was removed under vacuum to give the title compound as a brown solid (1.9 g, 54%, 95% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853214B2
Source datasetuspto-grants-2014_10
ORD IDord-9e73f97379574813b8ff767d2c420869
Source noteuspto-grants-2014_10