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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440706Generated: October 31, 2026

1-Benzylpiperazine → 5,6-Dihydro-2-(4-benzyl-1-piperazinyl)-4H-imidazo[4,5,1-ij]quinoline

https://huagongshe.com/reaction/1440706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolineHCID 15287105—
Product5,6-Dihydro-2-(4-benzyl-1-piperazinyl)-4H-imidazo[4,5,1-ij]quinolineHCID 1941983770%

Reaction Steps

A solution of 2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (3.00 g) in 1-benzylpiperazine (10 ml) was stirred at 100° C., under nitrogen, for four hrs. The reaction mixture was quenched with dilute sodium bicarbonate solution (300 ml) and extracted with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was purified by high performance liquid chromatography (silica gel; 25:1 dichloromethane-methanol). The appropriate fractions were collected and evaporated. The residue was recrystallized from ethyl acetate to give 3.6 g (70%) of product, mp 157°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500423
Source datasetuspto-grants-1996_03
ORD IDord-6056e77850404251aabf14895d71d1d1
Source noteuspto-grants-1996_03