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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923522Generated: October 31, 2026

Methyl iodide → HCID 118308718, compound

https://huagongshe.com/reaction/923522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 118308700HCID 118308700—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDimethylformamideHCID 6228—
ProductHCID 118308718HCID 11830871828.9%

Reaction Steps

To a solution of 245 mg of 8-[(2,6-difluorobenzyl)oxy]-N-[1-hydroxy-2-(2H-tetrazol-5-yl)propan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide in 5 ml of DMF were added 200 mg of potassium carbonate and 50 μl of methyl iodide, followed by stirring at room temperature for 2 hours. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography. To the obtained crude product were added isopropyl alcohol and diisopropyl ether, and the insoluble materials were collected by filtration and dried under reduced pressure to obtain 73 mg of 8-[(2,6-difluorobenzyl)oxy]-N-[1-hydroxy-2-(2-methyl-2H-tetrazol-5-yl)propan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide (Ex7a). Further, to the other crude product was added diisopropyl ether, and the insoluble materials were collected by filtration and dried under reduced pressure to obtain 27 mg of 8-[(2,6-difluorobenzyl)oxy]-N-[1-hydroxy-2-(1-methyl-1H-tetrazol-5-yl)propan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide (Ex7b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-e2b5f2b4cb4c4dc2a378d3f755836614
Source noteuspto-grants-2016_03