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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853412Generated: October 30, 2026

Water → 6,7-Dimethoxy-4-(5-indolinyloxy)quinoline

https://huagongshe.com/reaction/853412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylsilaneHCID 12052—
ReactantSodiumHCID 5360545—
Reactant4-[(1H-Indol-5-yl)oxy]-6,7-dimethoxyquinolineHCID 22132645—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
Product6,7-Dimethoxy-4-(5-indolinyloxy)quinolineHCID 2293644179.5%

Reaction Steps

After dissolving 6,7-dimethoxy-4-(5-indolyloxy)quinoline (30 mg, 0.0780 mmol, described in WO9717329, p.52) in trifluoroacetic acid (0.9 ml), triethylsilane (45 ml, 0.2808 mmol, 3.0 eqM) was added while cooling on ice, and the mixture was stirred for 4 hours and 30 minutes at room temperature under a nitrogen atmosphere. After cooling, the reaction solution was diluted with ethyl acetate, neutralized with saturated sodium bicarnobate water, extracted with ethyl acetate, washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/ethanol system) to obtain the title compound (20 mg, 0.0620 mmol, 66.28%) as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-444f5c4534214b3ab7cfc22a48ec19c9
Source noteuspto-grants-2007_08