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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923521Generated: October 29, 2026

Diisopropyl Ether → HCID 118308761, compound

https://huagongshe.com/reaction/923521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium chlorodifluoroacetateHCID 2734985—
ReactantHCID 131734991HCID 131734991—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 118308761HCID 11830876139.1%

Reaction Steps

To a mixture of 153 mg of potassium carbonate and 5 ml of DMF was added dropwise a solution of 346 mg of N-[1-{[tert-butyl (diphenyl)silyl]oxy}-2-(2H-tetrazol-5-yl)propan-2-yl]-8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxamide and 158 mg of sodium chloro(difluoro)acetate in 3 ml of DMF at an inner temperature of 95° C., followed by stirring at the same temperature for 1 hour. After leaving to be cooled to room temperature, water was added thereto, 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 ethyl acetate and diisopropyl ether, and the insoluble materials were collected by filtration and dried under reduced pressure to obtain 98 mg of 8-[(2,6-difluorobenzyl)oxy]-N-{2-[2-(difluoromethyl)-2H-tetrazol-5-yl]-1-hydroxypropan-2-yl}-2-methylimidazo[1,2-a]pyridine-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-9f52e547d2fb43d6b43b5b7bf4eefc9f
Source noteuspto-grants-2016_03