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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524857Generated: October 31, 2026

1-Methylpiperazine → 1-Methyl-4-(3-nitro-4-pyridyl)piperazine

https://huagongshe.com/reaction/524857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product1-Methyl-4-(3-nitro-4-pyridyl)piperazineHCID 86720915—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-chloro-3-nitro-pyridine (2 g, 12.61 mmol) in dioxane (15 mL) was treated with 1-methylpiperazine (1.515 g, 1.678 mL, 15.13 mmol) and DIPEA (2.445 g, 3.295 mL, 18.92 mmol). The mixture was stirred at 80° C. for 1 hour, cooled to RT. The mixture was partioned between EtOAc and an aqueous saturated solution of NaHCO3 (40 ml). Combined organic extract was dried over MgSO4 and concentrated under reduced pressure to give an orange oil which was purified by chromatography on silica eluting with 5-10% MeOH/EtOAc/0.5-1% NH4OH to give 1-methyl-4-(3-nitro-4-pyridyl)piperazine 14 as a deep yellow oil which crystallised on standing. (2.56 g, 11.52 mmol, 91.36%). MS (ES+) 223.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-13bf62e9aafb484a99b6a3547a3cc20f
Source noteuspto-grants-2016_05