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| | 3,4-Diamino-6-bromopyridine Basic information |
| Product Name: | 3,4-Diamino-6-bromopyridine | | Synonyms: | 3,4-Diamino-6-bromopyridine;6-Bromopyridine-3,4-diamine;6-broMopyridin-3,4-diaMine;3,4-Pyridinediamine, 6-bromo-;3,4-Diamino-6-bromopyridine ISO 9001：2015 REACH;6-Bromo-3,4-pyridinediamine | | CAS: | 1033203-41-6 | | MF: | C5H6BrN3 | | MW: | 188.03 | | EINECS: | | | Product Categories: | | | Mol File: | 1033203-41-6.mol |  |
| | 3,4-Diamino-6-bromopyridine Chemical Properties |
| Boiling point | 395.5±37.0 °C(Predicted) | | density | 1.818±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 4.94±0.42(Predicted) | | Appearance | Light yellow to brown Solid |
| | 3,4-Diamino-6-bromopyridine Usage And Synthesis |
| Synthesis | 2-Bromo-5-nitropyridin-4-amine (300.0 mg, 2.48 mmol) was used as starting material, which was added to acetic acid together with iron powder (300.0 mg, 5.37 mmol). The reaction mixture was stirred at 75 °C for 4 h and subsequently cooled to room temperature. The reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography with an eluent ratio of hexane: ethyl acetate = 50:50. The fraction containing the target product was collected and concentrated under reduced pressure to afford 6-bromopyridine-3,4-diamine (200.0 mg, 78% yield) as a brown solid.1H-NMR (400 MHz, DMSO-d6) data were as follows: δ 7.39 (s, 1H), 6.42 (s, 1H), 5.74 (brs, 2H), 4.66 (brs, 2H). | | References | [1] Patent: US2014/315888, 2014, A1. Location in patent: Paragraph 1233-1234 |
| | 3,4-Diamino-6-bromopyridine Preparation Products And Raw materials |
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