Basic information Safety Supplier Related

6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID

Basic information Safety Supplier Related

6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Basic information

Product Name:
6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
Synonyms:
  • 6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
  • 6-bromo-1H-imidazo[1,2-a]pyridine-8-carboxylic acid
  • 6-bromo-1H-imidazo[1,2-a]...
  • 2-a]pyridine-8-carboxylic acid
  • 6-broMoH-iMidazo[1
  • IMidazo[1,2-a]pyridine-8-carboxylic acid, 6-broMo-
  • 6-bromo-8-imidazo[1,2-a]pyridinecarboxylic acid
CAS:
903129-78-2
MF:
C8H5BrN2O2
MW:
241.04
Mol File:
Mol File
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6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Chemical Properties

Density 
1.89±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-1.37±0.41(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
43
Safety Statements 
36/37
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6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Usage And Synthesis

Synthesis

97-97-2

52833-94-0

903129-78-2

GENERAL STEPS: 2-Amino-5-bromonicotinic acid (5.0 g, 23.04 mmol) and sodium acetate (3.78 g, 46.1 mmol) were dissolved in 100 mL of a 60% aqueous ethanol solution under stirring conditions. Subsequently, a solution of 2-chloro-1,1-dimethoxyethane (5.74 g, 46.1 mmol) in water (6 mL) was added to this solution and concentrated hydrochloric acid (1.0 mL) was added dropwise. The reaction mixture was heated to reflux for 2.5 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and the residue was diluted with cold water and the pH adjusted to neutral (about 7) with saturated sodium bicarbonate solution. The reaction mixture was extracted with ethyl acetate (2 x 100 mL), the organic phases were combined, washed sequentially with water (2 x 100 mL) and brine (2 x 100 mL) and dried over anhydrous sodium sulfate. The crude product was purified by grinding with petroleum ether containing 2% ethyl acetate. 4.8 g of 6-bromoimidazo[1,2-a]pyridine-8-carboxylic acid was obtained in 86% yield. The product characterization data were as follows: 1H NMR (DMSO-d6, 300 MHz): δ 7.66 (d, 1H, J = 1.2 Hz, Ar), 7.79 (d, 1H, J = 1.5 Hz, Ar), 8.04 (s, 1H, Ar), 8.96 (d, 1H, J = 1.5 Hz, Ar); MS (ES+): m/e 242 (M + 1 ).

References

[1] Patent: WO2014/80241, 2014, A1. Location in patent: Page/Page column 41

6-BROMO-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACIDSupplier

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