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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788990Generated: November 3, 2026

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

https://huagongshe.com/reaction/1788990

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 numberUS04686228
Source datasetuspto-grants-1987_08
ORD IDord-a0355ae516294cdf811e5110b87ff144
Source noteuspto-grants-1987_08