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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420164Generated: October 25, 2026

Potassium Carbonate → Desfluoro Iloperidone (Impurity)

https://huagongshe.com/reaction/1420164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropoxy)-3-methoxyacetophenoneHCID 7314264—
Reactant4-(3-Benzisothiazolyl) piperidineHCID 13324093—
CatalystPotassium IodideHCID 4875—
SolventAcetonitrileHCID 6342—
ProductDesfluoro Iloperidone (Impurity)HCID 10024423109%

Reaction Steps

A mixture of 3-(4-piperidinyl)-1,2-benzisothiazole (3.0 g, 13.7 mmol), potassium carbonate (2.3 g, 16.5 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (4.0 g, 16.5 mmol), potassium iodide (200 mg) and acetonitrile (100 ml) was stirred at reflux under N2 for 24 hours. The cooled reaction was filtered and the cake was washed well with acetonitrile. The filtrate was concentrated to an oily residue, which was partitioned between water and ethyl acetate. The ethyl acetate extract was washed well with water, dried with MgSO4 and concentrated to yield 6.1 g of a beige oil which solidified upon standing. The product was triturated with diethyl ether and filtered to give 4.2 g of a beige solid. The compound was recrystallized from ethyl alcohol to afford 3.5 g, and another recrystallization from ethyl alcohol (utilizing decolonizing carbon) provided 2.4 g (41%) of 1-[4-[3-[4-(1,2-benzisothiazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone, m.p. 93°-95° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889004
Source datasetuspto-grants-1999_03
ORD IDord-56dfc77dc39741189dbef56891ef9591
Source noteuspto-grants-1999_03