HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350697Generated: October 29, 2026
Potassium Iodide → HCID 21973227, compound
https://huagongshe.com/reaction/350697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Reactant | HCID 21973229 | HCID 21973229 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21973227 | HCID 21973227 | 62.2% |
Reaction Steps
4.12 g (17.3 millimoles) of 5-(3-chloropropylamino)-2-methyl-2H-pyridazine-3-one-hydrochloride, 100 ml of acetonitrile, 4.29 g (19.5 millimoles) of 6-fluoro-3-piperidine-4-yl-1,2-benzisoxazole, 7.24 g of potassium carbonate and 0.39 g of potassium iodide are admixed. The reaction mixture is heated to boiling under stirring for 24 hours, cooled to room temperature and filtered. To the product 100 ml of water are added and the aqueous phase is extracted five times with 90 ml of dichloro methane each. The united organic phases are washed with a saturated sodium chloride solution; dried over magnesium sulfate and filtered over activated charcoal. The organic filtrate is evaporated in vacuo. The residue is suspended in diethyl ether and filtered. The crude product is recrystallized from acetonitrile. Thus 4.14 g of the desired compound are obtained. Yield 62.2%. M.p.: 163–165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183283B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-253581045e154580bbf9b9d394fe501a |
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| Source note | uspto-grants-2007_02 |
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