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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864643Generated: October 30, 2026

1-Methylpiperazine → HCID 15345718, compound

https://huagongshe.com/reaction/864643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 19419847HCID 19419847—
ProductHCID 15345718HCID 1534571857%

Reaction Steps

A solution of 7-bromo-2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (3.00 g) in N-methylpiperazine (20 ml) was stirred under reflux, under nitrogen, for two hrs. The reaction mixture was quenched with dilute sodium bicarbonate solution (200 ml) and extracted with chloroform. 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; 7:1 dichloromethane-methanol). The appropriate fractions were collected and evaporated. The residue was recrystallized from ethyl acetate-ether to give 2.1 g (57%) of product, mp 132°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563272
Source datasetuspto-grants-1996_10
ORD IDord-7f17b67110bc40968aaa746cf6be8a05
Source noteuspto-grants-1996_10