HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-bromo-4-methyl-3-nitropyridine → 5-Bromo-4-methylpyridine-2,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-bromo-4-methyl-3-nitropyridine | HCID 7213207 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5-Bromo-4-methylpyridine-2,3-diamine | HCID 10125141 | — |
Reaction Steps
2-Amino-5-bromo-4-methyl-3-nitropyridine (5 g) was dissolved in 6M HCl (50 mL) and iron powder was slowly added. The reaction was then heated to reflux until no starting material was seen via HPLC. The reaction was then cooled to room temperature and filtered. The bis-HCl salt was dried to a cream solid which was then taken up in EtOAc, neutralized with 50% NaOH solution to yield 5-bromo-4-methylpyridine-2,3-diamine as a free base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846664B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-50a004bff53548748da3cb000baa2d26 |
| Source note | uspto-grants-2014_09 |