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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374768Generated: November 1, 2026

Potassium Iodide → Ocaperidone

https://huagongshe.com/reaction/374768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantR-56109 hydrochlorideHCID 11334359—
ReactantHCID 18995805HCID 18995805—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductOcaperidoneHCID 7135147.6%

Reaction Steps

A mixture of 4.8 parts of 3-(2-bromoethyl)-2,9-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one, 3.9 parts of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole monohydrochloride, 10 parts of sodium carbonate, a few crystals of potassium iodide and 144 parts of 4-methyl-2-pentanone was stirred overnight at room temperature. After cooling, the reaction mixture was poured into water. The organic layer was separated, dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 95:5). The eluent of the desired fraction was evaporated and the residue was crystallized from acetonitrile, yielding 3 parts (47.6%) of 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2,9-dimethyl-4H-pyrido[1,2-a]-pyrimidin-4-one; mp. 199.9° C. (comp. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482943
Source datasetuspto-grants-1996_01
ORD IDord-97613a49ed404f53a6434082a6e6852a
Source noteuspto-grants-1996_01