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1033203-41-6

1033203-41-6 Structure

1033203-41-6 Structure
IdentificationBack Directory
[Name]

3,4-Diamino-6-bromopyridine
[CAS]

1033203-41-6
[Synonyms]

6-broMopyridin-3,4-diaMine
3,4-Diamino-6-bromopyridine
6-Bromopyridine-3,4-diamine
3,4-Pyridinediamine, 6-bromo-
3,4-Diamino-6-bromopyridine ISO 9001:2015 REACH
[Molecular Formula]

C5H6BrN3
[MDL Number]

MFCD11100655
[MOL File]

1033203-41-6.mol
[Molecular Weight]

188.03
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3,4-Diamino-6-bromopyridine(1033203-41-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-BROMO-5-NITROPYRIDIN-4-AMINE

84487-15-0

3,4-Diamino-6-bromopyridine

1033203-41-6

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
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