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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650534Generated: October 27, 2026

4-(Piperidin-1-yl)aniline → n-[4-(1-Piperidinyl)phenyl]benzo[g]quinolin-4-amine

https://huagongshe.com/reaction/650534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Piperidin-1-yl)anilineHCID 413501—
Reactant4-Chlorobenzo[g]quinolineHCID 12407978—
ReactantSodium t-butoxideHCID 23676156—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventTolueneHCID 1140—
Productn-[4-(1-Piperidinyl)phenyl]benzo[g]quinolin-4-amineHCID 283201485%

Reaction Steps

4-Chlorobenzo[g]quinoline (7b) (50 mg, 0.23 mmol), 4-(1-piperidino) aniline (50 mg, 1.2 equivalents), bis(1,5-cyclooctadiene)nickel(O) (Ni(COD)2 1.5 mg, 0.02 equivalents), 1,1′-bis(diphenylphosphino)ferrocene (DPPF, 5 mg, 0.04 equivalents) and sodium t-butoxide (31 mg, 1.4 equiv) in 2.5 mL of dry toluene were refluxed under a 5 nitrogen atmosphere until observed complete by TLC. The mixture was concentrated in vacuo and purified by flash chromatography (gradient: 50:50:2 to 60:40:2 hexane: EtOAc:Et3N) to provide 69 mg of clean N-[4-(1-piperidinyl)phenyl]benzo[g]quinolin-4-amine (8), 85% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274596B1
Source datasetuspto-grants-2001_08
ORD IDord-b35d11d2e2b7495894e00c5ac057f4eb
Source noteuspto-grants-2001_08