Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502378Generated: October 31, 2026

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

https://huagongshe.com/reaction/1502378

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 numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-1eee33be305c4130b3ec1ce960a9b22d
Source noteuspto-grants-2015_12