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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 121386233 | HCID 121386233 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-2-cyclopropyl-3-methylimidazo[1,2-a]pyrazine | HCID 89690355 | 80.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365540B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-f8544c1bf2f040de883c953ff768096d |
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| Source note | uspto-grants-2016_06 |
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