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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934983Generated: November 1, 2026

3-Iodoaniline → HCID 10223619, compound

https://huagongshe.com/reaction/1934983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-IodoanilineHCID 12271—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
ProductHCID 10223619HCID 1022361982.9%

Reaction Steps

A mixture of 3.10 ml (25.7 mmol) 3-iodoaniline, 200 ml ethanol, and 5.00 g (21.4 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile was heated to reflux under N2 for 3.5 hours. Cooled and made basic with a saturated sodium bicarbonate. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane and collected. Air dried, washed solids with water, and dried in vacuo. Dissolved solids in 400 ml ethyl acetate, stirred with Darco, filtered and removed solvent. Dried solids in vacuo to give 7.38 g of yellow solid: mass spectrum (electrospray m/e): M+H=417.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384051B1
Source datasetuspto-grants-2002_05
ORD IDord-6282d2ee0baf4e4ea70cfab859e536a4
Source noteuspto-grants-2002_05