Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206859Generated: November 1, 2026

Methyl iodide → 3-[(E)-{[(6-aminopyridin-2-yl)methoxy]imino}(phenyl)methyl]-4-methyl-1,2,4-oxadiazol-5(4H)-one

https://huagongshe.com/reaction/2206859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[(Z)-N-[(6-amino-2-pyridinyl)methoxy]-C-phenylcarbonimidoyl]-4H-1,2,4-oxadiazol-5-oneHCID 136626364—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product3-[(E)-{[(6-aminopyridin-2-yl)methoxy]imino}(phenyl)methyl]-4-methyl-1,2,4-oxadiazol-5(4H)-oneHCID 8944387786.8%

Reaction Steps

To a solution of 3-[(Z)-{[(6-aminopyridin-2-yl)methoxy]imino}(phenyl)methyl]-1,2,4-oxadiazol-5(4H)-one (1 g, 3.21 mmol, 1 eq.) in MeCN (50 ml) and DMF (10 ml) was added potassium carbonate (532 mg, 3.85 mmol, 1.2 eq.) followed by iodomethane (547 mg, 3.85 mmol, 1.2 eq.). The reaction was stirred at room temperature overnight. The reaction was quenched by addition of water and extracted with EtOAc (3×50 ml). The organics were combined, washed with aq. sat. NaCl, dried over MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 3-[(Z)-{[(6-aminopyridin-2-yl)methoxy]imino}(phenyl)methyl]-4-methyl-1,2,4-oxadiazol-5(4H)-one (906 mg, 85% yield) has a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09375010B2
Source datasetuspto-grants-2016_06
ORD IDord-c3e29ded53464c6984d9ff8c7e414d39
Source noteuspto-grants-2016_06