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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16771Generated: October 29, 2026

1-Methylpiperazine → 6-(4-Methylpiperazin-1-yl)pyridazine-3-carboxamide

https://huagongshe.com/reaction/16771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant6-Chloropyridazine-3-carboxamideHCID 12577557—
SolventIsopropanolHCID 3776—
Product6-(4-Methylpiperazin-1-yl)pyridazine-3-carboxamideHCID 2031679275.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

6-Chloropyridazine-3-carboxamide (0.315 g, 2 mmol) and 1-methylpiperazine (0.555 ml, 5.00 mmol) were suspended in 2-propanol (2.000 ml) and sealed into a microwave tube. The reaction was heated to 130° C. for 30 mins in the microwave reactor and cooled to ambient temperature. The resulting precipitate was collected by filtration, washed with 2-propanol (10 mL) and dried under vacuum to afford 6-(4-methylpiperazin-1-yl)pyridazine-3-carboxamide (0.333 g, 75%) as a white solid, which was used without further purification. A sample (100 mg) of the crude product was purified by preparative LCMS using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford 6-(4-methylpiperazin-1-yl)pyridazine-3-carboxamide (54 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-0489d8d2cba14143aa3b81f712ed2005
Source noteuspto-grants-2010_06