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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504492Generated: October 30, 2026

Water → Perfluorophenyl 1-(2-chloro-3'-fluoro-5-methoxy-[1,1'-biphenyl]-4-yl)-2-oxo-1,2-dihydroquinoline-6-sulfonate

https://huagongshe.com/reaction/1504492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-Dichloro-5,5-dimethylhydantoinHCID 8360—
ReactantTriethylamineHCID 8471—
ReactantPentafluorophenolHCID 13041—
Reactant6-(benzylthio)-1-(2-chloro-3'-fluoro-5-methoxy-[1,1'-biphenyl]-4-yl)quinolin-2(1H)-oneHCID 117737012—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductPerfluorophenyl 1-(2-chloro-3'-fluoro-5-methoxy-[1,1'-biphenyl]-4-yl)-2-oxo-1,2-dihydroquinoline-6-sulfonateHCID 11773725148.1%

Reaction Steps

A RBF was charged with 6-(benzylthio)-1-(2-chloro-3′-fluoro-5-methoxy-[1,1′-biphenyl]-4-yl)quinolin-2(1H)-one (1.00 g, 1.992 mmol), DCM (18.9 ml), acetic acid (0.47 ml), and water (0.47 ml) to give clear, orange solution. The flask was cooled in an ice-water bath for 10 min, then 1,3-dichloro-5,5-dimethylhydantoin (0.654 ml, 4.98 mmol) was added in one portion. After 30 min, 2,3,4,5,6-pentafluorophenol (0.417 ml, 3.98 mmol) and triethylamine (0.694 ml, 4.98 mmol) (dropwise) were added in sequence. After 2 hours, the mixture was diluted with water, then extracted with DCM (2×). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (40-g Redi-Sep Gold column, 25-g silica gel loading column, 0-50% EtOAc/Heptane) to give perfluorophenyl 1-(2-chloro-3′-fluoro-5-methoxy-[1,1′-biphenyl]-4-yl)-2-oxo-1,2-dihydroquinoline-6-sulfonate (0.600 g, 0.959 mmol, 48.1% yield) as an off-white solid. m/z (ESI) 626.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-4ceb58869c544c27a78a641812631fbc
Source noteuspto-grants-2015_12