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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424434Generated: November 1, 2026

Piperazine → N-(2-Cyclobutylethyl)-6-(1-piperazinyl)-3-pyridazinecarboxamide

https://huagongshe.com/reaction/2424434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant6-CHLOROPYRIDAZINE-3-CARBOXYLIC Acid (2-CYCLOBUTYLETHYL)AMIDEHCID 86026045—
SolventAcetonitrileHCID 6342—
ProductN-(2-Cyclobutylethyl)-6-(1-piperazinyl)-3-pyridazinecarboxamideHCID 6684936578.8%

Reaction Steps

To a solution of 6-chloropyridazine-3-carboxylic acid (2-cyclobutylethyl)-amide (1.2 g, 5.00 mmol) in acetonitrile (40 mL) was added piperazine (1.29 g, 15.00 mmol). The reaction mixture was heated to reflux overnight. The mixture was evaporated and the solid residue was taken in ethyl acetate (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined ethyl acetates were dried over Na2SO4 and concentrated in vacuo to give the title compound as yellow solid (1.14 g, 78.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964591B2
Source datasetuspto-grants-2011_06
ORD IDord-a0b7c5386a9147fb806ce2458b855676
Source noteuspto-grants-2011_06