Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908991Generated: October 29, 2026

Iodine → 6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-one

https://huagongshe.com/reaction/1908991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
ReactantButylamineHCID 8007—
Reactant6-chloro-7-methoxy-2-methylquinolin-4(1H)-oneHCID 49781464—
SolventDimethylformamideHCID 6228—
Product6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-oneHCID 6701670289%

Reaction Steps

To a stirred solution of 6-chloro-7-methoxy-2-methylquinolin-4(1H)-one (6.43 g, 28.7 mmol) and n-butylamine (28 ml, 287 mmol) in dimethylformamide (57 ml) cooled by a room temperature water bath was added iodine (7.30 g, 28.7 mmol) in a saturated solution of aqueous potassium iodide (29 ml). The reaction mixture was stirred 12 hours at room temperature. Residual iodine was quenched with 0.1 M aqueous sodium thiosulfate, and the resulting solution was concentrated in vacuo. The residue was resuspended in water and filtered to give 8.93 g (89% yield) of 6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-one as a light brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598354B2
Source datasetuspto-grants-2013_12
ORD IDord-02c63bc650d64ef1a6497d9fb85a30e3
Source noteuspto-grants-2013_12