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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 6-Chloro-N-methylnicotinamide | HCID 12364230 | — |
| Product | 3-Pyridinecarboxamide, N-methyl-6-(4-methyl-1-piperazinyl)- | HCID 3042937 | 1,011.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297375B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-6810dfee7f7142a2820c706e17a20f72 |
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| Source note | uspto-grants-2001_10 |
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