HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397558Generated: October 31, 2026
Potassium Iodide → HCID 23000344, compound
https://huagongshe.com/reaction/397558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | HCID 23000329 | HCID 23000329 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23000344 | HCID 23000344 | 29.6% |
Reaction Steps
796 mg of 6-[6-(methanesulfonyloxy)hexylamino][1,2,4]triazolo[4,3-b]pyridazine was dissolved in 15 ml of N,N-dimethylformamide; 769 mg of 1-(diphenylmethyl)piperazine, 422 mg of potassium carbonate, and 506 mg of potassium iodide were added, followed by stirring at 60° C. for 4 hours. After cooling, saline was added; the reaction mixture was extracted with ethyl acetate and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (50:5:1). The desired fraction was collected and concentrated under reduced pressure; the residue was crystallized from ethyl acetate, washed with diethyl ether, recrystallized in the same manner, and dried, to yield 353 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610694B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-a0f779fe2b494fb3b125a2c3938e003b |
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| Source note | uspto-grants-2003_08 |
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