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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 6-Chloropyridazine-3-carboxamide | HCID 12577557 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-(4-Methylpiperazin-1-yl)pyridazine-3-carboxamide | HCID 20316792 | 75.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737149B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-0489d8d2cba14143aa3b81f712ed2005 |
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| Source note | uspto-grants-2010_06 |
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