HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457007Generated: October 27, 2026
Ethylamine → 3-Bromo-N-ethylimidazo[1,2-a]pyrazin-8-amine
https://huagongshe.com/reaction/457007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3,5-Dibromoimidazo[1,2-a]pyrazine | HCID 14207592 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-N-ethylimidazo[1,2-a]pyrazin-8-amine | HCID 10399418 | 53% |
Reaction Steps
3,5-Dibromo-imidazo[1,2-a]pyrazine (D) (200 mg, 0.722 mol) was added to 2M ethylamine in THF (10.8 ml, 30 eq.). The mixture was heated at 70° C. in sealed tube for 8 hr. The mixture was then cooled to rt, and diluted with DCM (100 ml) and water (50 ml). The organic layer was washed with brine, dried and concentrated. The residue was purified on a silica gel column to give 92.2 mg (yield 53%) of (3-bromo-imidazo[1,2-a]pyrazin-8-yl)-ethyl-amine as a crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186832B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-a060667cf24a460ea0905cd3a4e3075e |
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| Source note | uspto-grants-2007_03 |
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