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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395322Generated: October 26, 2026

Tetrahydrofuran → 2-(4-Aminophenylthio)-4-phenylquinoline

https://huagongshe.com/reaction/2395322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-AminothiophenolHCID 14510—
Reactant2-Chloro-4-phenylquinolineHCID 2306687—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
Product2-(4-Aminophenylthio)-4-phenylquinolineHCID 18971678451.6%

Reaction Steps

2-Chloro-4-phenylquinoline (4.18 mmoles, 10.0 g), 4-aminothiophenol (41.8 mmoles, 5.2 g) and DMAP (41.8 mmoles, 5.0 g) were stirred in 200 ml ethanol and 50 ml THF for 3 days. The solution was concentrated, ethyl acetate added, washed with water, dried over sodium sulfate and the solvent removed. The product was purified by HPLC over silica gel eluted with 30% ethyl acetate in hexane to yield 2-(4-aminophenylthio)-4-phenylquinoline 6.2 g, 45%. Mass Spec (FD) 328. Calculated for C21H16N2S: C, 76.80; H, 4.91N, 8.53. Found: C, 77.04; H, 5.00; N, 8.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814646
Source datasetuspto-grants-1998_09
ORD IDord-9e34b9533c9b498faec1d6283cca03f7
Source noteuspto-grants-1998_09