Basic information Safety Supplier Related

2-Amino-5-bromonicotinaldehyde

Basic information Safety Supplier Related

2-Amino-5-bromonicotinaldehyde Basic information

Product Name:
2-Amino-5-bromonicotinaldehyde
Synonyms:
  • 2-Amino-5-bromonicotinaldehyde
  • 2-Amino-5-bromopyridine-3-carboxaldehyde, 2-Amino-5-bromo-3-formylpyridine
  • 2-AMino-5-broMonicotildehyde
  • 2-AMINO-5-BROMOPYRIDINE-3-CARBOXALDEHYDE
  • 2-AMino-5-broMo-pyridine-3-carbaldehyde
  • 3-Pyridinecarboxaldehyde, 2-aMino-5-broMo-
  • 2-aMino-5-broMo-3-pyridinecarbaldehyde
  • 2-Amino-5-bromonicotinaldehyde 98%
CAS:
206997-15-1
MF:
C6H5BrN2O
MW:
201.02
Mol File:
206997-15-1.mol
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2-Amino-5-bromonicotinaldehyde Chemical Properties

Melting point:
167-169
Boiling point:
300.5±42.0 °C(Predicted)
Density 
1.782±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.74±0.49(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

Hazard Codes 
Xi
RIDADR 
UN 2811 6.1 / PGIII
HazardClass 
IRRITANT
HS Code 
2933399990
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2-Amino-5-bromonicotinaldehyde Usage And Synthesis

Synthesis

7521-41-7

206997-15-1

General procedure for the synthesis of 2-amino-5-bromonicotinaldehyde from 2-amino-3-pyridinecarboxaldehyde: A. To a solution of 2-aminopyridine-3-carbaldehyde (10.1 g, 81.0 mmol) in acetonitrile (150 mL) was added N-bromosuccinimide (15.1 g, 84.0 mmol). The reaction mixture was stirred under reflux conditions for 2 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was filtered. The collected solid was washed with methanol and subsequently dried under vacuum to afford 2-amino-5-bromopyridine-3-carbaldehyde as a brown solid in 79% yield (12.9 g). 1H NMR (400 MHz, CDCl3): δ 9.81 (s, 1H), 8.30 (d, J = 2.4 Hz, 1H), 7.89 (d, J = 2.4 Hz, 1H), 6.78 (br s, 2H).

References

[1] Patent: WO2015/81257, 2015, A2. Location in patent: Page/Page column 61-62
[2] Journal of Polymer Science, Part A: Polymer Chemistry, 2011, vol. 49, # 19, p. 4204 - 4212
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 21, p. 8777 - 8791
[4] Patent: WO2013/82756, 2013, A1. Location in patent: Page/Page column 21; 30-31
[5] Patent: WO2009/115788, 2009, A1. Location in patent: Page/Page column 54

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