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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452820Generated: October 30, 2026

Potassium Iodide → N-methyl-1-[5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazol-2-yl]methylamine

https://huagongshe.com/reaction/452820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethylamine tetrahydrofuranHCID 66615946—
ReactantHCID 68663800HCID 68663800—
SolventEthyl AcetateHCID 8857—
ProductN-methyl-1-[5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazol-2-yl]methylamineHCID 6866341267%

Reaction Steps

A mixture of 2-(chloromethyl)-5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole (0.30 g, 0.76 mmol), potassium iodide (0.13 g, 0.76 mmol) and 2M methylamine-tetrahydrofuran solution (10 mL) was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=7/3) and recrystallized from hexane/diisopropyl ether to give the title compound (0.20 g, yield 67%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-79c7902c08d8409ca77cb3298bf28585
Source noteuspto-grants-2013_07