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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440699Generated: November 3, 2026

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

https://huagongshe.com/reaction/1440699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolineHCID 15287105—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product5,6-Dihydro-2-(4-methyl-1-piperazinyl)-4H-imidazo[4,5,1-ij]quinolineHCID 1534571670%

Reaction Steps

A solution of 2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (4.30 g) in 20 ml of N-methylpiperazine (18.06 g) was heated under reflux, under nitrogen, with stirring. After 30 mins, the solution was diluted with sodium bicarbonate solution (100 ml) and water (200 ml). The aqueous solution was extracted with chloroform. The organic phase was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by high performance liquid chromatography (silica gel; methanol). The appropriate fractions were collected and evaporated. The residue was crystallized from ether-petroleum ether to give 4.0 g (70%) of product, mp 112°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500423
Source datasetuspto-grants-1996_03
ORD IDord-15c36759bb614c2987caf405cd69131a
Source noteuspto-grants-1996_03