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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203016Generated: November 1, 2026

Trifluoroacetic anhydride → 6-Bromo-2-cyclopropyl-3-methylimidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/2203016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 121386233HCID 121386233—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-2-cyclopropyl-3-methylimidazo[1,2-a]pyrazineHCID 8969035580.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of N-(5-bromo-1-(1-cyclopropyl-1-oxopropan-2-yl)pyrazin-2(1H)-ylidene)-4-methylbenzenesulfonamide (1.24 g) in THF (10 ml) was added trifluoroacetic anhydride (1.23 g) at 0° C., and the mixture was heated at 60° C. for 3 h. The mixture was partitioned between EtOAc and saturated NaHCO3 solution, and the organic layer was washed with 1 M NaOH and brine successively, dried over MgSO4, concentrated in vacuo, and purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (593 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-f8544c1bf2f040de883c953ff768096d
Source noteuspto-grants-2016_06