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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468861Generated: October 31, 2026

Iodine chloride → 7-Chloro-3-(2-chlorophenyl)-4-iodo-2,6-naphthyridine 2-oxide

https://huagongshe.com/reaction/468861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
Reactant2-Chloro-5-((2-chlorophenyl)ethynyl)isonicotinaldehyde oximeHCID 136413189—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product7-Chloro-3-(2-chlorophenyl)-4-iodo-2,6-naphthyridine 2-oxideHCID 86674953—

Reaction Steps

To a slurry of 2-chloro-5-((2-chlorophenyl)ethynyl)isonicotinaldehyde oxime (850 mg, 2.9 mmol) in acetonitrile (8 mL) was added iodine monochloride (1.4 g, 8.8 mmol). The reaction mixture instantly became homogeneous and was stirred at room temperature. After 15 minutes the reaction mixture was diluted with ethyl acetate (100 mL) and washed with water (100 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford an orange residue that was used in the next step without further purification (1.2 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623889B2
Source datasetuspto-grants-2014_01
ORD IDord-3abd70d1455f4a8a8821edb2264c2e87
Source noteuspto-grants-2014_01