HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959419Generated: November 3, 2026
Hydrazine hydrate (1:1) → 3-Amino-6-bromopyrazine-2-carbohydrazide
https://huagongshe.com/reaction/1959419
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | 94% |
Reaction Steps
To a suspension of methyl 3-amino-6-bromo-pyrazine-2-carboxylate (2.5 g, 10.8 mmol) in EtOH (50 mL) was added hydrazine hydrate (3.2 g, 3.1 mL, 64.6 mmol) and the reaction mixture was heated at 70° C. for 1.5 h forming a thick yellow solid. The solid was isolated by filtration, washed with water (20 mL) and ethanol (40 mL). The solid was dried under high vacuum to yield 3-amino-6-bromo-pyrazine-2-carbohydrazide (2.35 g, 94%) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 9.78 (s, 1H), 8.31 (s, 1H), 7.62 (s, 2H), 4.53 (d, =3.5 Hz, 2H). LC/MS m/z 233.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410112B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c7c5bc9710e146c785144800cdc36850 |
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| Source note | uspto-grants-2013_04 |
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