HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181028Generated: October 25, 2026
Hydrochloric Acid → 6-Bromopyridine-2,3-diamine
https://huagongshe.com/reaction/2181028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Bromo-3-nitro-2-pyridinamine | HCID 12097745 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromopyridine-2,3-diamine | HCID 22388386 | 47.9% |
Reaction Steps
To a suspension of 2-amino-6-bromo-3-nitropyridine (21.8 g) in ethanol (220 ml)-water (22 ml) was added iron powder (39.0 g) at room temperature. Conc. hydrochloric acid (0.8 ml) was added and the mixture was gradually heated with stirring to start the reaction. The mixture was refluxed under heating for 2 hr, and an insoluble matter was removed by filtration while hot. The solvent was evaporated under reduced pressure, and water (200 ml) and active charcoal were added to the resulting solid, which was followed by heating. The insoluble matter was removed by filtration while hot, and water was evaporated under reduced pressure from the filtrate to give 2,3-diamino-6-bromopyridine (9.00 g) as a green brown powder. To the resulting solid from the above reaction were added ethanol (100 ml)-water (100 ml) and the mixture was heated for dissolution. The insoluble matter was removed by filtration. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/3) to further give the objective compound (8.25 g) as a black powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06890934B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-771a50a3abd247518d81beb7501a4269 |
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| Source note | uspto-grants-2005_05 |
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