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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431411Generated: November 4, 2026

Potassium Carbonate → 4-chloro-5,7-difluoro-3-methyl-2-(1-methyl-1H-indol-5-yl)quinoline

https://huagongshe.com/reaction/1431411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indoleHCID 16217778—
Reactant2,4-Dichloro-5,7-difluoro-3-methylquinolineHCID 59631040—
SolventTolueneHCID 1140—
Product4-chloro-5,7-difluoro-3-methyl-2-(1-methyl-1H-indol-5-yl)quinolineHCID 59631214—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 2,4-dichloro-5,7-difluoro-3-methylquinoline (1.0 g, 4.03 mmol) in toluene (8.1 mL) was added 1-methylindole-5-boronic acid pinacol ester (1.037 g, 4.03 mmol), potassium carbonate (1.67 g, 12.09 mmol) and palladium tetrakistriphenylphosphine (0.466 g, 0.403 mmol). The reaction was stirred at 100° C. and stirring continued for 16 h. The reaction mixture was cooled to rt and concentrated in vacuo. The crude material was purified by column chromatography on silica gel, eluting with 0-50% EtOAc in hexanes to provide 4-chloro-5,7-difluoro-3-methyl-2-(1-methyl-1H-indol-5-yl)quinoline as a clear solid. Mass Spectrum (ESI) m/e=343.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-0f634aff091d4648a325e2ec0b5d5bff
Source noteuspto-grants-2015_01