HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217211Generated: October 29, 2026
6-nitropyridin-2-amine → HCID 56923659, compound
https://huagongshe.com/reaction/217211
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-nitropyridin-2-amine | HCID 2762881 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 56923659 | HCID 56923659 | 153.3% |
Reaction Steps
To a stirred solution of 6-nitro-pyridin-2-ylamine (1.0 g, 7.18 mmol) in CH3CN (100 mL), protected from light and under nitrogen atmosphere, N-bromosuccinamide (636 mg, 3.59 mmol) was added at 0° C. After 1 hour, another portion of N-bromosuccinamide (636 mg, 3.59 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirring was continued overnight. The reaction mixture was then quenched by the addition of saturated aqueous Na2S2O3 and extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with water, brine, dried over MgSO4 (anhydrous) and concentrated in vacuo. The crude product was purified by Biotage using 10% ethyl acetate in hexane to afford 1.2 g of 5-bromo-6-nitro-pyridin-2-ylamine (10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193363B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-10b20d1264f743f08f34014207046a02 |
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| Source note | uspto-grants-2012_06 |
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