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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926473Generated: November 2, 2026

Dichloromethane → 3-(4-(1H-Imidazol-1-yl)benzyl)-2,4-dichloro-6-iodoquinoline

https://huagongshe.com/reaction/926473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178517226HCID 178517226—
SolventAcetonitrileHCID 6342—
Product3-(4-(1H-Imidazol-1-yl)benzyl)-2,4-dichloro-6-iodoquinolineHCID 118006287—

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture containing 3-(4-(1H-imidazol-1-yl)benzyl)-6-iodoquinoline-2,4-diol (3.0 g, 6.8 mmol, Intermediate 17: step a) and phosphorus oxychloride (1.9 mL, 20 mmol) in acetonitrile (34 mL) was heated to 100° C. After 16 hours, the flask was allowed to cool to 23° C. Dichloromethane (200 mL) and saturated aqueous sodium bicarbonate solution were added in sequence and the resulting biphasic mixture was stirred for 30 minutes. The biphasic mixture was filtered through Celite® and the layers of the biphasic filtrate were separated. The organic layer was dried with magnesium sulfate and the dried solution was filtered. Silica gel (7 g) was added to the filtrate and the solvent was removed by rotary evaporation to afford a free-flowing powder. The powder was loaded onto a column of silica gel for purification. Elution with dichloromethane initially, grading to 5% methanol-dichloromethane provided the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-97bc11b1c4e44a3aa83fd9229a35d43a
Source noteuspto-grants-2016_03