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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365309Generated: October 31, 2026

Potassium Iodide → HCID 23291085, compound

https://huagongshe.com/reaction/365309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(1-Piperazinylmethyl)quinolineHCID 4375313—
ReactantHCID 23291097HCID 23291097—
SolventDimethylformamideHCID 6228—
ProductHCID 23291085HCID 23291085—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture consisting of 7-(3-chloropropoxy)-3,4-dihydro-2H-1,4-benzothiazin-3-one-1-oxide (2.02 g, 7.38 mmol), N-(2-quinolylmethyl)piperazine (2.52 g, 11.07 mmol), potassium carbonate (2.04 g, 14.76 mmol), potassium iodide (2.45 g, 14.76 mmol) and DMF (50 ml) was stirred at 80° C. for 4 hours. The solvent was distilled off from the reaction mixture under reduced pressure, followed by the addition of water. The resulting mixture was extracted with chloroform-methanol (10:1). The extract was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column while using chloroform-ammonia-saturated methanol (10:1) as an eluent. Fractions containing the target compound were collected and then concentrated under reduced pressure, whereby 1.23 g of the title compound was obtained as a yellow oil (4.49 mmol, 60.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127360
Source datasetuspto-grants-2000_10
ORD IDord-3376ad834f6d4f3eb24a02d96a54ef7e
Source noteuspto-grants-2000_10