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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853378Generated: October 27, 2026

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

https://huagongshe.com/reaction/853378

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 bicarnobate 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 numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-d2d75124c25d4d5ca0d7a0c601777600
Source noteuspto-grants-2007_08