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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60382Generated: October 29, 2026

Trifluoroacetic anhydride → 2-Cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/60382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantN-(1-(1-Cyclopropyl-1-oxopropan-2-yl)-5-iodopyridin-2(1H)-ylidene)-4-methylbenzenesulfonamideHCID 131735781—
SolventTetrahydrofuranHCID 8028—
Product2-Cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridineHCID 89690398—

Reaction Steps

To a solution of N-(1-(1-cyclopropyl-1-oxopropan-2-yl)-5-iodopyridin-2(1H)-ylidene)-4-methylbenzenesulfonamide (30.5 g) in THF (300 mL) was added trifluoroacetic anhydride (18.3 mL) dropwise, and the mixture was stirred for 3 hr. The resulting precipitate was collected by filtration, and washed with diethyl ether to give a salt of the title compound as a white solid. The obtained solid was dissolved in 1 N sodium hydroxide, and the solution was extracted with ethyl acetate/THF. Then the organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The obtained solid was washed with diisopropyl ether to give the title compound (17.7 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440987B2
Source datasetuspto-grants-2016_09
ORD IDord-6db0c35485e640179f32a44cfd03d72d
Source noteuspto-grants-2016_09