Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561046Generated: November 1, 2026

4-Fluorophenylboronic acid → 7-Chloro-3-(4-chloro-benzenesulfonyl)-4-(4-fluoro-phenyl)-quinoline

https://huagongshe.com/reaction/561046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant4-Bromo-7-chloro-3-(4-chloro-benzenesulfonyl)-quinolineHCID 67000154—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
Product7-Chloro-3-(4-chloro-benzenesulfonyl)-4-(4-fluoro-phenyl)-quinolineHCID 2516852167.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-bromo-7-chloro-3-(4-chloro-benzenesulfonyl)-quinoline (0.42 g, 1 mmol), 4-fluorophenylboronic acid (0.21 g, 1.5 mmol) and tetrakis-(triphenylphosphin)palladium(0) (0.08 g, 0.07 mmol) in 30 ml 1,2-dimethoxyethane and 8 ml of 2M aqueous sodium carbonate solution was stirred for 2 hours at 70° C. After cooling the mixture was concentrated in vacuo. The crude residue was purified by column chromatography on silica gel (Kieselgel 60, eluent: chloroform) and crystallized from methanol to obtain 0.29 g of the title compound in 67% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063220B2
Source datasetuspto-grants-2011_11
ORD IDord-0a25ebb70ce944ccb556e2193e04c014
Source noteuspto-grants-2011_11