HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749050Generated: October 30, 2026
Hydrazine → 3-Amino-6-bromopyrazine-2-carbohydrazide
https://huagongshe.com/reaction/1749050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Methyl 3-Amino-6-bromopyrazine-2-carboxylate | HCID 227251 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-6-bromopyrazine-2-carbohydrazide | HCID 58070256 | 101% |
Reaction Steps
Hydrazine hydrate (23.59 mL, 480.75 mmol) was added dropwise to a stirred mixture of methyl 3-amino-6-bromopyrazine-2-carboxylate (100 g, 418.04 mmol) in EtOH (2 L). The mixture was heated at 50° C. under nitrogen. The resulting thick suspension was stirred at 50° C. for 16 hours. Further hydrazine (2.5 mL) was added in one portion and the suspension was stirred at 50° C. for a further 24 hours. Ethanol (500 mL) was charged to the thick reaction mixture and the mixture was allowed to cool to room temperature. The resulting suspension was filtered and the solid washed with ethanol (1 L) and dried in vacuo to give 3-amino-6-bromopyrazine-2-carbohydrazide (98 g, quantitative) as a cream solid: 1H NMR Spectrum: (DMSO-d6) 4.52 (2H, s), 7.59 (2H, s), 8.30 (1H, s), 9.74 (1H, s): Mass Spectrum [M+H]+=232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09155727B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-f664cd355a22464593e2aa6a05a32d98 |
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| Source note | uspto-grants-2015_10 |
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