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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248404Generated: October 25, 2026

Potassium Iodide → 3-{1-[4,4-bis-(4-Fluorophenyl)-1-butyl]-4-piperidinyl}-1,2-benzisothiazole hydrochloride

https://huagongshe.com/reaction/1248404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-(4-Chlorobutylidene)bis(4-fluorobenzene)HCID 76820—
Reactant4-(3-Benzisothiazolyl) piperidineHCID 13324093—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-{1-[4,4-bis-(4-Fluorophenyl)-1-butyl]-4-piperidinyl}-1,2-benzisothiazole hydrochlorideHCID 2025575321%

Reaction Steps

A mixture of 5.0 g of 3-(4-piperidinyl)-1,2-benzisothiazole, 7.70 g of 4-chloro-1,1-bis(4-fluorophenyl)butane, 7.0 g of potassium carbonate, 0.25 g of potassium iodide and 120 ml of dimethylformamide was stirred at 90° for 8.0 hrs and overnight at ambient temperature. The reaction mixture was poured into water, extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The product was purified by high-pressure liquid chromatography using dichloromethane:methanol (2%) as the eluent. The eluent was evaporated, the residue was dissolved in ether and a saturated hydrogen chloride/ether solution was added dropwise to yield a solid. The solid was recrystallized from ethyl acetate/ether to give 2.0 g (21%) of product, mp 198°-199°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04524074
Source datasetuspto-grants-1985_06
ORD IDord-b39b42f96a684cba825d9dc67b616f5a
Source noteuspto-grants-1985_06