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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350697Generated: October 29, 2026

Potassium Iodide → HCID 21973227, compound

https://huagongshe.com/reaction/350697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
ReactantHCID 21973229HCID 21973229—
SolventAcetonitrileHCID 6342—
ProductHCID 21973227HCID 2197322762.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183283B2
Source datasetuspto-grants-2007_02
ORD IDord-253581045e154580bbf9b9d394fe501a
Source noteuspto-grants-2007_02