ChemicalBook--->CAS DataBase List--->114414-17-4

114414-17-4

114414-17-4 Structure

114414-17-4 Structure
IdentificationBack Directory
[Name]

2-AMINO-3-HYDROXY-4-BROMOPYRIDINE HBR
[CAS]

114414-17-4
[Synonyms]

2-AMino-3-hydroxy-4-broMopydine HBr
2-AMINO-3-HYDROXY-4-BROMOPYRIDINE HBR
2-Amino-4-bromo-3-hydroxypyridine hbr
2-amino-4-bromo-3-pyridinol hydrobromide
2-AMino-4-broMopyridin-3-ol hydrobroMide
2-Amino-4-bromo-3-pyridinol monohydrobromide
2-AMINO-3-HYDROXY-4-BROMOPYRIDINE HYDROBROMIDE
[Molecular Formula]

C5H6Br2N2O
[MDL Number]

MFCD09842810
[MOL File]

114414-17-4.mol
[Molecular Weight]

269.922
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

crystalline solid
[color ]

Very dark red
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]

2-AMINO-3-HYDROXY-4-BROMOPYRIDINE HBR(114414-17-4)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-Amino-3-hydroxypyridine

16867-03-1

2-AMINO-3-HYDROXY-4-BROMOPYRIDINE HBR

114414-17-4

General procedure for the synthesis of 2-amino-4-bromopyridin-3-ol hydrobromide from 2-amino-3-hydroxypyridine: Bromine (11.2 mL, 0.21 mol) was slowly added dropwise to a mechanically stirred suspension of 2-amino-3-hydroxypyridine (20 g, 0.18 mol) in acetic acid (300 mL) at 5-10 °C, after which the reaction system was brought to room temperature. The reaction mixture was heated to 120-125 °C, maintained for 12 h and then concentrated to give the crude product. The crude product was ground with ether (50 mL x 3) and subsequently dried under vacuum to afford 2-amino-4-bromopyridin-3-ol hydrobromide as a dark brown solid, which could be used in subsequent reactions without further purification. Yield: 48.5 g; MS (m/z): 189.3, 191.1 ([M + H]+).

[References]

[1] Patent: WO2018/42362, 2018, A1. Location in patent: Page/Page column 125
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