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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381867Generated: October 31, 2026

Potassium Iodide → 5,6,7,8-Tetradehydro Risperidone

https://huagongshe.com/reaction/1381867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-(2-Chloroethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 817866—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product5,6,7,8-Tetradehydro RisperidoneHCID 1437204019%

Reaction Steps

A mixture of 3.3 parts of 3-(2-chloroethyl)-2-methyl-4H-pyrido-[1,2-a]pyrimidin-4-one, 3.3 parts of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole, 8 parts of sodium carbonate, 1 part of potassium iodide and 120 parts of 4-methyl-2-pentanone was stirred and refluxed for 3 hours. The reaction mixture was cooled, water was added and the layers were separated. The organic phase was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 4-methyl-2-pentanone, yielding 1.2 parts (19%) of 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one; mp. 170.4° C. (compound 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804663
Source datasetuspto-grants-1989_02
ORD IDord-95e14a1c0633427398c6746e719dcfb6
Source noteuspto-grants-1989_02