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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657112Generated: October 31, 2026

Potassium Iodide → HCID 19801313, compound

https://huagongshe.com/reaction/1657112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(2-Pyrimidinyl)piperazineHCID 88747—
ReactantHCID 19786560HCID 19786560—
SolventDimethylformamideHCID 6228—
ProductHCID 19801313HCID 1980131338.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution consisting of 5-(3-chloropropyl)-3-(2-fluorophenyl)-6,7-dihydro-1,2-benzisoxazol-4(5H)-one (7.3 g) and DMF (100 ml) was added anhydrous potassium carbonate (1.6 g), diisopropylethyl amine (6.2 ml), 1-(2-pyrimidyl) piperazine (5.8 g) and potassium iodide (0.4 g) at room temperature with stirring. The flask was flushed with nitrogen and warmed to 80° C. for 16 hours. Upon cooling to room temperature, water and ethyl acetate were added to the reaction mixture. The layers were separated and the aqueous phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with water twice, then brine and dried (MgSO4). Filtration and concentration gave the crude product. Purification via flash column chromatography (silica gel, 2% triethylamine/ether) afforded 4.0 g of 6,7-dihydro-3-(2-fluorophenyl)-5-[3-(4-(2-pyrimidyl) -1-piperazinyl)-propyl]-1,2-benzisoxazo1-4(5H)-one as an oil which solidified upon standing. Recrystalization with ether gave the product as a solid, m.p. 115°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256672
Source datasetuspto-grants-1993_10
ORD IDord-1690954df2ae40ea9eb03a748310a7ce
Source noteuspto-grants-1993_10