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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778286Generated: October 29, 2026

4-Toluenesulfonyl chloride → 4-bromo-6-((4-chlorophenyl)(thiazol-2-yl)methyl)quinolin-2(1H)-one

https://huagongshe.com/reaction/1778286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-Bromo-6-((4-chlorophenyl)(thiazol-2-yl)methyl)quinoline 1-oxideHCID 118324015—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium CarbonateHCID 10340—
Product4-bromo-6-((4-chlorophenyl)(thiazol-2-yl)methyl)quinolin-2(1H)-oneHCID 118324003—

Reaction Steps

p-Toluenesulfonyl chloride (628 mg, 3.293 mmol, 1.5 equip) was added to a biphasic mixture of 4-bromo-6-((4-chlorophenyl)(thiazol-2-yl)methyl)quinoline 1-oxide in dichloromethane (6 mL) and 10% Na2CO3 (42 mL) and the resulting mixture stirred for 1 h. The reaction mixture was diluted with dichloromethane and water, the layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organic extracts were dried over Na2SO4, filtered, and concentrated. The residue was purified by MPLC to yield 4-bromo-6-((4-chlorophenyl)(thiazol-2-yl)methyl)quinolin-2(1H)-one as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266835B2
Source datasetuspto-grants-2016_02
ORD IDord-3d2599b416094221b30a7971c4db2e80
Source noteuspto-grants-2016_02