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2-Amino-5-bromoisonicotinic acid

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2-Amino-5-bromoisonicotinic acid Basic information

Product Name:
2-Amino-5-bromoisonicotinic acid
Synonyms:
  • 2-Amino-5-bromoisonicotinic acid
  • 2-Amino-5-bromo-4-pyridinecarboxylic acid
  • 2-aMino-5-broMopyridin-4-carboxylic acid
  • 4-Pyridinecarboxylic acid,2-amino-5-bromo-
  • 2-Amino-5-bromoisonicotinic
  • 2-Amino-5-bromoisonicotinicaci
  • 2-Amino-5-bromoisonicotinic acid ISO 9001:2015 REACH
CAS:
1000339-23-0
MF:
C6H5BrN2O2
MW:
217.02
EINECS:
202-303-5
Mol File:
1000339-23-0.mol
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2-Amino-5-bromoisonicotinic acid Chemical Properties

Boiling point:
464.1±45.0 °C(Predicted)
Density 
1.909
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
1.16±0.10(Predicted)
form 
solid
color 
Yellow
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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2-Amino-5-bromoisonicotinic acid Usage And Synthesis

Synthesis

882499-87-8

1000339-23-0

General procedure for the synthesis of 2-amino-5-bromo-4-carboxylic acid pyridine from 2-amino-5-bromoisonicotinic acid methyl ester: 2-amino-5-bromoisonicotinic acid methyl ester (10.0 g, 43.28 mmol) and lithium hydroxide (LiOH, 5.46 g, 129.8 mmol) were reacted with 2-amino-5-bromo-4-carboxylic acid methyl ester (10.0 g, 43.28 mmol) and 2-amino-5-bromoisonicotinic acid methyl ester (10.0 g, 43.28 mmol) and lithium hydroxide (LiOH, 5.46 g, 129.8 mmol) in a water (100 mL) in a solvent mixture of tetrahydrofuran (THF, 400 mL), methanol (MeOH, 200 mL), and water (100 mL), and the reaction was stirred at 70 °C for 2 h under nitrogen (N2) protection. Upon completion of the reaction, the reaction mixture was cooled to 0 °C and the pH was adjusted to 6 by dropwise addition of concentrated aqueous hydrochloric acid (HCl).Subsequently, the resulting suspension was filtered and the solid was dried under vacuum to afford pyridine 2-amino-5-bromo-4-carboxylic acid (7.8 g, 83% yield). The product was analyzed by liquid chromatography-mass spectrometry (LC-MS, ESI) and showed m/z 211 [M + H]+.

References

[1] Patent: WO2012/58125, 2012, A1. Location in patent: Page/Page column 145

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