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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55062Generated: October 25, 2026

4-Aminothiophenol → 2-(4-Aminophenylthio)-4-ethoxycarbonylquinoline

https://huagongshe.com/reaction/55062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminothiophenolHCID 14510—
ReactantEthyl 2-chloroquinoline-4-carboxylateHCID 230586—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
Product2-(4-Aminophenylthio)-4-ethoxycarbonylquinolineHCID 1897164636%

Reaction Steps

2-Chloro-4-ethoxycarbonylquinoline (0.024 moles, 5.56 g), 4-aminothiophenol (0.024 moles, 3.0 g) and 4-dimethylaminopyridine (0.024 moles, 2.9 g) were stirred in 250 ml ethanol for 3 days. The reaction mixture was filtered, concentrated, ethyl acetate added, washed with water and dried over sodium sulfate. The solution was concentrated and the product purified by HPLC over silica gel eluted with 25% ethyl acetate/hexane to yield 2-(4-aminophenylthio)-4-ethoxycarbonylquinoline 2.8 g, 36%. Mass Spec (FD) 324. Calculated for C18H16N2O2S: C, 66.64; H, 4.97; N, 8.63. Found: C, 66.50; H, 5.00 N, 8.54.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624937
Source datasetuspto-grants-1997_04
ORD IDord-603b04cd056d463f8fd093942204d27e
Source noteuspto-grants-1997_04