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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734039Generated: October 30, 2026

Potassium Iodide → HCID 67725547, compound

https://huagongshe.com/reaction/1734039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochlorideHCID 11521711—
ReactantHCID 21471973HCID 21471973—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 67725547HCID 67725547—

Reaction Conditions

Temperature60 °C

Reaction Steps

The mixture of 2.0 g of 4-(1,2-benzisothiazol-3-yl)piperazine hydrochloride, 2.0 g of 3-(4-chlorobutyryl)-2-methyl-5,6,7,8-tetrahydro-4H-thieno[3,2-c]azepin-4-one, 2.1 g of potassium carbonate and 1.2 g of potassium iodide in 15 ml of N,N-dimethylformamide and 15 ml of toluene was stirred at 60° C. for 3 hours. After the mixture was cooled in a water bath, water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with saline solution, dried over magnesium sulfate and concentrated. The residue was purified by column chromatography on a silica gel, dissolved in isopropyl alcohol and ethanol-maleic acid was added thereto to make maleate. The resulting crystals were recrystallized from ethanol to give 0.90 g of 3-(4-(4-(1,2-benzisothiazol-3-yl) piperazin-1-yl)butyryl)-2-methyl-5,6,7,8-tetrahydro-4H-thieno[3,2-c]azepin-4-one maleate as white crystals, m.p. 150°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532240
Source datasetuspto-grants-1996_07
ORD IDord-cf8ef10632034a1d935dbbd45318ca93
Source noteuspto-grants-1996_07