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2-Bromo-5-hydroxypyrazine

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2-Bromo-5-hydroxypyrazine Basic information

Product Name:
2-Bromo-5-hydroxypyrazine
Synonyms:
  • 5-BROMO-2-PYRAZINOL
  • 5-BROMO-2-HYDROXYPYRAZINE
  • 5-BROMO-2-HYDROXYPYRAZINE,5-BROMO-2-PYRAZINOL
  • 5-bromopyrazin-2-ol
  • 5-bromopyrazin-2-o
  • 2(1H)-Pyrazinone, 5-bromo- 2-Bromo-5-hydroxypyrazine
  • 5-Bromopyrazin-2(1H)-one
  • 2-hydroxy-5-bromopyrazine
CAS:
374063-92-0
MF:
C4H3BrN2O
MW:
174.98
Product Categories:
  • Piperazine series
  • Building Blocks
  • Pyrazine
  • Building Blocks/Intermediates
Mol File:
374063-92-0.mol
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2-Bromo-5-hydroxypyrazine Chemical Properties

Melting point:
115-119°C
Density 
2.00±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
10.02±0.40(Predicted)
form 
Crystalline Powder
color 
White to light brown
InChI
InChI=1S/C4H3BrN2O/c5-3-1-7-4(8)2-6-3/h1-2H,(H,7,8)
InChIKey
ITTXBHQAWOFJAI-UHFFFAOYSA-N
SMILES
C1(=O)NC=C(Br)N=C1
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-41
Safety Statements 
26-39
WGK Germany 
1
HS Code 
29339900
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2-Bromo-5-hydroxypyrazine Usage And Synthesis

Uses

5-bromo-1H-pyrazin-2-one is a useful research chemical.

Synthesis

59489-71-3

374063-92-0

General procedure for the synthesis of 2-bromo-5-hydroxypyrazine from 2-amino-5-bromopyrazine: sodium nitrite (1.35 g, 19.53 mmol) was added to concentrated sulfuric acid (9.8 mL) in batches at 0 °C. The mixture was heated to 50 °C until the sodium nitrite was completely dissolved and subsequently cooled to 0 °C. A solution of 5-bromo-pyrazin-2-ylamine (2.57 g, 14.68 mmol) in concentrated sulfuric acid (14.7 mL) was added slowly and dropwise. The ice bath was removed and the mixture was gradually warmed to room temperature and stirred for 15 minutes, followed by heating to 45 °C for 7 minutes. Upon completion of the reaction, it was cooled to room temperature and the reaction mixture was slowly poured into crushed ice water (100 mL). The pH of the aqueous phase was adjusted to 4 with 20% aqueous sodium hydroxide, followed by extraction with ethyl acetate (3 x 100 mL). The organic phases were combined, washed with water (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give 2-bromo-5-hydroxypyrazine (1.88 g, 73% yield) as a yellow solid. The product was characterized by 1H NMR (CDCl3, 300 MHz): δ 8.07 (1H, s), 7.62 (1H, d, J=3.0 Hz).

References

[1] Patent: US2005/187266, 2005, A1
[2] Patent: WO2004/92145, 2004, A1. Location in patent: Page 133
[3] Patent: US2010/29650, 2010, A1. Location in patent: Page/Page column 64
[4] Patent: US2005/9838, 2005, A1. Location in patent: Page 150
[5] Journal of Chemical Research, 2005, # 11, p. 747 - 749

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