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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387855Generated: October 27, 2026

Thioanisole → 6-Methoxy-4-[(5-nitro-2-thienyl)sulfanyl]-7-quinolinol

https://huagongshe.com/reaction/387855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
Reactant2-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]sulfanyl}-5-nitrothiopheneHCID 58931211—
SolventTrifluoroacetic acidHCID 6422—
Product6-Methoxy-4-[(5-nitro-2-thienyl)sulfanyl]-7-quinolinolHCID 13598995885.7%

Reaction Steps

7-(Benzyloxy)-6-methoxy-4-[(5-nitro-2-thienyl)sulfanyl]quinoline (4.0 g), trifluoroacetic acid (40 ml) and thioanisole (4 ml) were stirred together at 65° C. for 2 hours. The mixture was returned to room temperature, the solvent was distilled off under reduced pressure, 80 ml of methanol was added to the residue, and then bicarbonate water was added until the foaming subsided. The precipitated solid was filtered out to obtain 2.7 g of a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-6783fb8da877465aa3c6bdcbfec98a04
Source noteuspto-grants-2013_02