Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433508Generated: October 31, 2026

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

https://huagongshe.com/reaction/1433508

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 numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-502c745422ea4f8195af7b0f2be43548
Source noteuspto-grants-2009_11