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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356396Generated: October 31, 2026

Piperazine → 6-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amide

https://huagongshe.com/reaction/2356396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamideHCID 16733786—
SolventAcetonitrileHCID 6342—
Product6-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amideHCID 6684932288%

Reaction Steps

A solution of 6-chloropyridazine-3-carboxylic acid (3-methylbutyl)amide (2.52 g, 11.0 mmol) and piperazine (2.83 g, 32.8 mmol) in acetonitrile (30 mL) was heated to refluxed for 2 hours. The solvent was removed by evaporation, the residue was dissolved in water (50 ml) and extracted with dichloromethane (3×100 mL). The organic extract was dried over anhydrous Na2SO4 and then evaporated. The residue was passed through a pad of silica gel and concentrated to give 6-piperazin-1-yl-pyridazine-3-carboxylic acid (3-methylbutyl)amide (2.68 g, 88% yield). MS (ES+) m/z 278 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759348B2
Source datasetuspto-grants-2010_07
ORD IDord-ec1820d2ee444ce5bc93a7ddb9afb64c
Source noteuspto-grants-2010_07