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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108818Generated: November 1, 2026

N-Iodosuccinimide → HCID 22120912, compound

https://huagongshe.com/reaction/1108818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 22120896HCID 22120896—
SolventAcetonitrileHCID 6342—
ProductHCID 22120912HCID 22120912—

Reaction Steps

To a stirred solution of 5-amino-3-cyano-1-(2,6-dichlorophenyl)pyrazole (0.1318 g) in acetonitrile (5 ml) at room temperature was added N-iodosuccinimide (0.1469 g). Stirring was continued for 1 hour and the mixture was then evaporated to dryness. The residue was taken up in dioxane (5 ml). Furan-2-boronic acid (0.1232 g), tetrakis(triphenylphosphine)palladium(0) (0.0554 g) and a solution of potassium carbonate (0.4405 g) in water (2 ml) were added. The mixture was heated under reflux for 48 hours, then cooled and partitioned between ether and water. The separated aqueous layer was extracted with ether and the combined ether layers were washed with brine, dried and evaporated. The green oily residue was purified by column chromatography on silica gel (4 g) eluted with dichloromethane. Combination and evaporation of suitable fractions followed by recrystallisation from toluene gave the title compound as a light brown solid, m.p. 222.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069157
Source datasetuspto-grants-2000_05
ORD IDord-e6c3f9b89bb54760a4545a2800d69dad
Source noteuspto-grants-2000_05