Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294840Generated: October 30, 2026

Potassium Iodide → HCID 21471809, compound

https://huagongshe.com/reaction/2294840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantR-56109 hydrochlorideHCID 11334359—
ReactantHCID 21471776HCID 21471776—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 21471809HCID 2147180945.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 800 mg of 2-chloroethyl-4,5,6,7-tetrahydro-8H-thieno[2,3-c]azepin-8-one, 920 mg of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine hydrochloride, 1.45 g of potassium carbonate and 580 mg of potassium iodide in 10 ml of dimethylformamide and 10 ml of toluene was stirred at 90° C. for 22 hours and concentrated in vacuo. To the residue were added ethyl acetate and water, and separated. The ethyl acetate layer was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on a silica gel and recrystallized from ethyl acetate to give 0.65 g of 2-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-8H-thieno[2,3-c]azepin-8-one, m.p. 192°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691330
Source datasetuspto-grants-1997_11
ORD IDord-9d990a0568674070a183f3d29309839b
Source noteuspto-grants-1997_11