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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468303Generated: November 2, 2026

Triethylamine → HCID 86710135, compound

https://huagongshe.com/reaction/1468303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant3,3-Difluoroazetidine hydrochlorideHCID 2758247—
ReactantHCID 86710134HCID 86710134—
SolventAcetonitrileHCID 6342—
ProductHCID 86710135HCID 8671013594%

Reaction Conditions

Temperature50 °C

Reaction Steps

7-Bromo-2-isopropylimidazo[1,2-a]pyridine-3-sulfonylchloride (500 mg, 1.481 mmol) obtained in step 1 was dissolved in acetonitrile (5.0 mL), and the solution was stirred at 50° C. for 30 minutes after adding 3,3-difluoroazetidine hydrochloride (230 mg, 1.78 mmol) and triethylamine (0.413 ml, 2.96 mmol). The reaction mixture was allowed to cool to room temperature, and a sodium hydrogen carbonate aqueous solution was added. The precipitated solid was collected by filteration to give 7-bromo-3-(3,3-difluoroazetidin-1-ylsulfonyl)-2-isopropylimidazo[1,2-a]pyridine (546 mg, yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000186B2
Source datasetuspto-grants-2015_04
ORD IDord-f809d4ca10604c079b61ee048ebee3c2
Source noteuspto-grants-2015_04