HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486450Generated: October 30, 2026
Potassium Iodide → 3-Chloro-6-[4-(2-fluorophenyl)piperazin-1-yl]pyridazine
https://huagongshe.com/reaction/486450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | 1-(2-Fluorophenyl)piperazine | HCID 70529 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-6-[4-(2-fluorophenyl)piperazin-1-yl]pyridazine | HCID 15124549 | 77% |
Reaction Steps
A mixture of 3.1 parts of 3,6-dichloropyridazine, 3 parts of 1-(2-fluorophenyl)piperazine. 3.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 72 parts of N,N-dimethylformamide was stirred and heated over weekend at 60° C. The reaction mixture was poured into water. The precipitated product Was filtered off and dissolved in trichloromethane. The organic layer was dried, filtered and evaporated. The residue was purified by filtration over silica gel using a mixture of trichloromethane and methanol (98:2 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 2,2'-oxybispropane, yielding 4.5 parts (77%) of 3-chloro-6-[4-(2-fluorophenyl)-1-piperazinyl]pyridazine; mp. 148.0° C. (compound 9).
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-3542152fd698442586319937f5996f8e |
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| Source note | uspto-grants-1994_03 |
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