HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201570Generated: October 26, 2026
Bromine → 3-Amino-6-bromopyrazine-2-carboxamide
https://huagongshe.com/reaction/2201570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Aminopyrazine carboxamide | HCID 280292 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Amino-6-bromopyrazine-2-carboxamide | HCID 470899 | 95% |
Reaction Steps
To a stirred solution of 3-aminopyrazine-2-carboxamide (1 g, 7.24 mmol, prepared according to International Patent Application Publication No. WO2011054922) and NaOAc (200 mg, 2.44 mmol) in HOAc (15 mL) was added Br2 (0.45 mL) dropwise at 0° C. for 1 hour, and then it was stirred at 50° C. for 8 hours. After the mixing, it was poured into ice-water and filtrated, the crude product of 3-amino-6-bromopyrazine-2-carboxamide as brown solid (1.5 g, yield: 95%) was obtained. 1H-NMR (DMSO-d6, 400 MHz) δ 8.30 (s, 1H), 7.93 (s, 2H), 7.66 (s, 2H). MS (M+H)+: 217/219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09364482B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-2a914bcbf20e4df0a7dbaf10d9f167cb |
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| Source note | uspto-grants-2016_06 |
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