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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387890Generated: October 31, 2026

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

https://huagongshe.com/reaction/387890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantCarbonic acid--water (1/1)HCID 21993411—
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 bicarbonate water, extracted with ethyl acetate, washed with saturated saline 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 numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-63624380e9f8407a9cc4ac5aa83ac07b
Source noteuspto-grants-2013_02