HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486459Generated: October 28, 2026
3,6-Dichloropyridazine → HCID 19095533, compound
https://huagongshe.com/reaction/486459
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19095533 | HCID 19095533 | 45.3% |
Reaction Steps
A mixture of 3.3 parts of 3.6-dichloropyridazine, 3.3 parts of 1-(2-pyridinyl)piperazine. 1.5 parts of sodium hydrogencarbonate and 120 parts of ethanol was stirred and refluxed over weekend. The reaction mixture was evaporated. Water was added to the residue and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanol and tetrahydrofuran, yielding 2.5 parts (45.3%) of 3-chloro-6-[4-(2-pyridinyl)-1-piperazinyl]pyridazine; mp. 194.7° C. (compound 213).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292738 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-bf36a5459c3043c7811befb0211ebefb |
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| Source note | uspto-grants-1994_03 |
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