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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726368Generated: November 1, 2026

Piperazine → 6-(Piperazin-1-yl)pyridin-2-amine

https://huagongshe.com/reaction/1726368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Amino-6-chloropyridineHCID 206246—
ReactantSodium t-butoxideHCID 23676156—
CatalystHCID 178424406HCID 178424406—
SolventM-XyleneHCID 7929—
Product6-(Piperazin-1-yl)pyridin-2-amineHCID 152909765.3%

Reaction Steps

To a solution of 6-chloro-2-pyridinylamine (406 mg, 3.16 mmol) and piperazine (381 mg, 4.42 mmol) in m-xylene (10 ml), were added sodium tert-butoxide (425 mg, 4.42 mmol) and bis-(tri-o-tolylphosphine)palladium(II) dichloride (124 mg, 0.158 mmol). The mixture was heated at reflux under N2 for 24 h. The reaction was cooled down and tetrahydrofuran (THF, 10 ml) added, and the mixture was filtered on a celite pad. The filtrate was evaporated and purified via flash chromatography (CH2Cl2/MeOH/NH4OH) affording 30 mg of 2-amino-6-(piperazin-1-yl)pyridine (intermediate “Ia”) as a tan solid (5% yield). H-NMR (CD3OD): 2.95 (m, 4H), 3.47 (m, 4H), 5.93 (m, 1H), 6.01 (m, 1H), 7.24 (m, 1H). M+=179.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491821B2
Source datasetuspto-grants-2009_02
ORD IDord-93a3e0854ea24bb88a4dcf0d68a94237
Source noteuspto-grants-2009_02