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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55095Generated: October 26, 2026

2-(4-Nitrophenylthio)quinoline → 2-(4-Aminophenylthio)quinoline

https://huagongshe.com/reaction/55095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Nitrophenylthio)quinolineHCID 18971643—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product2-(4-Aminophenylthio)quinolineHCID 2263713093%

Reaction Steps

2-(4-Nitrophenylthio)quinoline (0.42 moles, 12.0 g) was hydrogenated in 300 ml DMF over 5.0 g Pd/C for 3 hr at room temperature. The solution was filtered through celite and concentrated. The product was triturated with ether and hexane to yield 2-(4-aminophenylthio)quinoline 10.0 g, 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624937
Source datasetuspto-grants-1997_04
ORD IDord-cf4c99fe053f41b9ab5b2ac5ab6a9af3
Source noteuspto-grants-1997_04