HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350696Generated: October 30, 2026
Potassium Iodide → HCID 21973236, compound
https://huagongshe.com/reaction/350696
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 22339777 | HCID 22339777 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21973236 | HCID 21973236 | 55.9% |
Reaction Steps
3.67 g (16.4 millimoles) of 5-(2-chloroethylamino)-2-methyl-2H-pyridazine-3-one-hydrochloride, 90 ml of acetonitrile, 4.05 g (18.4 millimoles) of 6-fluoro-3-piperidine-4-yl-1,2-benzisoxazole, 6.84 g of potassium carbonate and 0.37 g of potassium iodide are admixed. The reaction mixture is stirred under heating to boiling 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 50.0 ml of dichloro methane each. The united organic phases are washed with water, dried over anhydrous magnesium sulfate, filtered and the organic phase is evaporated in vacuo. The residue is suspended in diethyl ether and filtered. The crude product is recrystallized from acetonitrile. Thus 3.4 g of the desired compound are obtained. Yield 55.9%.
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-c1051382d16847cda4ae4bb7953ce608 |
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| Source note | uspto-grants-2007_02 |
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