Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379369Generated: October 27, 2026

1-Methylpiperazine → 3-Pyridinecarboxamide, N-methyl-6-(4-methyl-1-piperazinyl)-

https://huagongshe.com/reaction/379369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant6-Chloro-N-methylnicotinamideHCID 12364230—
Product3-Pyridinecarboxamide, N-methyl-6-(4-methyl-1-piperazinyl)-HCID 30429371,011.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 52.0 g (30.5 mmol) 6-chloro-N-methyl-nicotinamide and 176 ml (1.58 mol) 1-methylpiperazine was heated at 100° C. for 1.5 h in an autoclave. After cooling to room temperature excess 1-methylpiperazine was removed by distillation. The residue was partitioned in 1000 ml dichloromethane/1 N aqueous sodium hydroxide solution. The layers were separated and the aqueous layer was extracted with three 500 ml portions of dichloromethane. Concentration and short column chromatography yielded 72.3 g (97%) of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297375B1
Source datasetuspto-grants-2001_10
ORD IDord-6810dfee7f7142a2820c706e17a20f72
Source noteuspto-grants-2001_10