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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845418Generated: November 1, 2026

Chloroform → 4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline

https://huagongshe.com/reaction/845418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinolineHCID 13359991—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinolineHCID 1406899851.2%

Reaction Steps

4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinoline (6.2 g) in ethanol (300 ml) with 5% Pd/C catalyst was stirred at 50° under an atmosphere of hydrogen (50 p.s.i.) for 20 hours. The mixture was cooled, chloroform (100 ml) added and the solution filtered through "Solkafloc". The solid was washed with chloroform-methanol (1:1, 4×100 ml) and the combined filtrates evaporated in vacuo. The residue was partitioned between chloroform-sodium carbonate solution (10%), the organic layer removed, the aqueous phase saturated with salt and further extracted with chloroform. The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to yield 4-amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline (2.42 g). Spectroscopy showed this product to be the same as that of Example 32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758568
Source datasetuspto-grants-1988_07
ORD IDord-ec2bdd80d6d7450c9242452e0547daa8
Source noteuspto-grants-1988_07