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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206861Generated: October 26, 2026

Potassium Iodide → HCID 178465692, compound

https://huagongshe.com/reaction/2206861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant(Iodomethyl)cyclopropaneHCID 2763048—
ReactantHCID 178465699HCID 178465699—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178465692HCID 17846569211.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of N′-hydroxy-N-{6-[({[(Z)-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}ethanimidamide (150 mg, 0.392 mmol, 1 eq), iodomethylcyclopropane (0.069 ml, 0.588 mmol, 1.5 eq) and cesium carbonate (191 mg, 0.588 mmol, 1.5 eq) in DMF (3 ml) was stirred at 80° C. for 7 h and overnight at room temperature. Iodomethylcyclopropane (0.069 ml, 0.588 mmol, 1.5 eq), cesium carbonate (191 mg, 0.588 mmol, 1.5 eq) and potassium iodide (0.1 eq) were then added and the mixture was stirred at 60° C. for 8 h. Water was added and the mixture was extracted with ethyl acetate. The organics were combined, dried over MgSO4 and evaporated. The residue was purified by chromatography on silica gel to afford N′-(cyclopropylmethoxy)-N-{6-[({[(Z)-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}ethanimidamide (20 mg, 10% yield) as a transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09375010B2
Source datasetuspto-grants-2016_06
ORD IDord-e91eb2bf19414ab3b845cd8e889ffd3d
Source noteuspto-grants-2016_06