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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186492Generated: November 1, 2026

1-Methylpiperazine → HCID 86670919, compound

https://huagongshe.com/reaction/1186492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86670917HCID 86670917—
SolventIsopropanolHCID 3776—
ProductHCID 86670919HCID 86670919—

Reaction Steps

A mixture of 3-(6-bromo-pyridin-2-yl)-8-chloro-imidazo[1,2-a]pyrazine (from Example 38 supra) (1.44 g, 4.65 mmol), 1-methylpiperazine (2.1 g, 21 mmol), and diisopropylethylamine (2.7 g, 21 mmol) in 2-propanol (300 mL) was stirred and heated at reflux overnight. The solution was then cooled to room temperature, concentrated under reduced pressure. The resulted solid was washed with water, partitioned between CH2Cl2 and brine. The organic layer was dried over Na2SO4 and filtered. The filtrate was concentrated under reduced pressure. The crude product was purified by chromatography (CH2Cl2:CH3OH, 100:1) to give 3-(6-bromo-pyridin-2-yl)-8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazine. (Yield 1.27 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-0ec757afcb0b41faa58b2172679a888b
Source noteuspto-grants-2014_03