HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072791Generated: October 25, 2026
Hydrogen Bromide → 6-Bromo-3-nitro-2-pyridinamine
https://huagongshe.com/reaction/1072791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 6-Chloro-3-nitropyridin-2-ylamine | HCID 2724035 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Bromo-3-nitro-2-pyridinamine | HCID 12097745 | — |
Reaction Steps
A 30% solution of hydrogen bromide in acetic acid (10 ml) was added to 2-amino-6-chloro-3-nitropyridine (1.0 g) at room temperature and the mixture was heated at 100° C. After 24 hr, a 30% solution of hydrogen bromide in acetic acid (5 ml) was added. After 48 hr, the reaction mixture was cooled and concentrated. The residue was neutralized with 28% aqueous ammonia and extracted three times with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was crystallized from isopropyl ether to give the objective compound (1.14 g) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06911469B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-4bd694c7b0a84d14bc5a8ab1317d6890 |
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| Source note | uspto-grants-2005_06 |
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