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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440705Generated: October 30, 2026

1-Piperazinecarboxaldehyde → 4-[5,6-Dihydro-4H-imidazo[4,5,1-ij]quinolin-2-yl]-1-piperazinecarboxaldehyd

https://huagongshe.com/reaction/1440705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperazinecarboxaldehydeHCID 82191—
Reactant2-Chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolineHCID 15287105—
Product4-[5,6-Dihydro-4H-imidazo[4,5,1-ij]quinolin-2-yl]-1-piperazinecarboxaldehydHCID 1941983864.5%

Reaction Steps

A solution of 2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (20.00 g) in 1-piperazinecarboxaldehyde (25.00 g) was stirred at 120° C., under nitrogen, for 1.5 hrs. The reaction mixture was quenched with dilute sodium bicarbonate solution (300 ml) and extracted with chloroform. The organic extracts were combined, washed with brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated. The residue was purified by flash chromatography (silica gel; 25:1 dichloromethane-methanol). The appropriate fractions were collected and evaporated. The residue was recrystallized twice from ethyl acetate to give 18.1 g (64%) of product, mp 138°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500423
Source datasetuspto-grants-1996_03
ORD IDord-1114f059c1ea4e69ba7780c4c44ca06e
Source noteuspto-grants-1996_03