Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720396Generated: October 25, 2026

Quinoline → HCID 9842061, compound

https://huagongshe.com/reaction/720396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
Reactant4-(Pyrrolidin-1-yl)phenacyl bromideHCID 3681785—
ReactantHCID 21892109HCID 21892109—
SolventAcetonitrileHCID 6342—
ProductHCID 9842061HCID 984206196%

Reaction Steps

1-(4-Pyrrolidin-1-yl-phenacyl)-quinolinium bromide: A stirred solution of 2-bromo-1-(4-pyrrolidin-1-yl-phenyl)-ethanone (689 mg, 2.57 mmol), quinoline (250 μL, 2.11 mmol) and acetonitrile (5.0 mL) was refluxed at 96° C. for 7 h under argon. The solution was equilibrated to room temperature and the precipitate was filtered on a Buchner funnel. The solid was dried in vacuo to yield 812 mg (96%) of the title compound. 1H NMR (DMSO-d6): 9.49 (d, J=4.67 Hz, 1H), 9.42 (d, J=8.25 Hz, 1H), 8.54 (d, J=8.24 Hz, 1H), 8.30 (m, 2H), 8.22 (td, J=7.92, 1.31 Hz, 1H), 8.06 (t, J=7.41 Hz, 1H), 7.96 (d, J=8.79 Hz, 2H), 6.84 (s, 2H), 6.72 (d, J=9.07 Hz, 2H), 3.40 (t, J=6.31 Hz, 4H), 2.02 (t, J=6.46 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135480B2
Source datasetuspto-grants-2006_11
ORD IDord-0f83fcb3b954434cb7a265029378d581
Source noteuspto-grants-2006_11