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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847391Generated: October 31, 2026

Potassium Iodide → HCID 19881143, compound

https://huagongshe.com/reaction/847391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Piperazinylpyrimidine dihydrochlorideHCID 11680272—
ReactantHCID 19881056HCID 19881056—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 19881143HCID 1988114351.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4.1 g of 4-(4-chlorobutyl)-2,3-dihydrothieno[3,2-f]-1,4-thiazepin-5(4H)-one 1,1-dioxide in 80 ml of a mixed solvent of N,N-dimethylformamide and toluene (1:1) were added 3.2 g of N-(2-pyrimidinyl)piperazine dihydrochloride, 3.8 g of potassium carbonate and 2.3 g of potassium iodide and the mixture was stirred for 3 hours at 90° C. Then, the mixture was poured into water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and the solvent was distilled off. The resulting residue was chromatographed on a silica gel and eluted using chloroform and methanol (95:5) as an eluent. The resulting crystals were recrystallized from ethanol to give 3.0 g of 2,3-dihydro-4-[4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl]thieno[3,2-f]-1,4-thiazepin-5(4H)-one 1,1-dioxide as white crystals, melting at 161°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05141930
Source datasetuspto-grants-1992_08
ORD IDord-7be4b1e662664f65ac96f74a55046d83
Source noteuspto-grants-1992_08