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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202833Generated: October 31, 2026

Trifluoroacetic anhydride → p-Toluenesulfonic acid

https://huagongshe.com/reaction/2202833

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—
Productp-Toluenesulfonic acidHCID 6101—
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-methylbenzene sulfonamide (30.5 g) in THF (300 ml) was added trifluoroacetic anhydride (18.3 ml) dropwise. After 3 h, the resulting precipitate was collected by filtration, and washed with ether to give p-toluenesulfonic acid salt of the title compound as a white solid. The solid obtained was dissolved in a mixture of 1 M NaOH, EtOAc and THF. Then the organic layer was washed with brine, dried over MgSO4 and concentrated. The resulting solid was triturated with IPE, and collected to give the title compound (17.7 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-938062ca7cf144798bd98ab7d67b0abb
Source noteuspto-grants-2016_06