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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010242Generated: November 4, 2026

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

https://huagongshe.com/reaction/1010242

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 sodium 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 numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-3791ea923c1f487aa28eff692c44372e
Source noteuspto-grants-2011_07