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3-Amino-2-bromo-4,6-dimethylpyridine

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3-Amino-2-bromo-4,6-dimethylpyridine Basic information

Product Name:
3-Amino-2-bromo-4,6-dimethylpyridine
Synonyms:
  • IFLAB-BB F1371-0213
  • 2-BROMO-4,6-DIMETHYL-PYRIDIN-3-YLAMINE
  • AKOS BBS-00005796
  • 3-AMINO-2-BROMO-4,6-DIMETHYLPYRIDINE
  • 5-Amino-2-bromo-4,6-dimethylpyridine
  • 2-bromo-4,6-dimethylpyridin-3-amine
  • 3-Amino-2-bromo-4,6-dimethylpyridine ,98%
  • 2-Bromo-4,6-dimethylpyridin-3-amine, 5-Amino-6-bromo-2,4-lutidine
CAS:
104829-98-3
MF:
C7H9BrN2
MW:
201.06
Product Categories:
  • Heterocycles
  • Heterocyclic Compound
  • Pyridine series
  • Heterocyclic Compounds
  • Amines
  • Pyridines
Mol File:
104829-98-3.mol
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3-Amino-2-bromo-4,6-dimethylpyridine Chemical Properties

Melting point:
61-62 °C
Boiling point:
304.8±37.0 °C(Predicted)
Density 
1.504±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
3.09±0.18(Predicted)
color 
Light orange
CAS DataBase Reference
104829-98-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
HS Code 
2933399990
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3-Amino-2-bromo-4,6-dimethylpyridine Usage And Synthesis

Synthesis

610261-09-1

104829-98-3

Bromine (2.8 g, 17.5 mmol) was added slowly dropwise to an aqueous solution (21 mL) of sodium hydroxide (2.1 g, 52.5 mmol) at -5 °C. Subsequently, 2-bromo-4,6-dimethylpyridine-3-carboxamide (3.19 g, 14 mmol) was added all at once. The reaction mixture was first stirred at 0 °C for 1 h, then warmed up to 70 °C and continued stirring for 1 h. The reaction was carried out at 0 °C for 1 h. The reaction mixture was then cooled to 70 °C. After completion of the reaction, the mixture was cooled to room temperature. Extraction was carried out with dichloromethane and the organic layer was washed with saturated brine and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate, 2:1) to afford the target product 3-amino-2-bromo-4,6-dimethylpyridine (2.8 g, 100% yield) as a light yellow solid.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 5093 - 5097
[2] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 395 - 408,14
[3] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 395 - 408
[4] Organic Letters, 2008, vol. 10, # 21, p. 4895 - 4898
[5] Journal of Organic Chemistry, 2010, vol. 75, # 3, p. 716 - 725

3-Amino-2-bromo-4,6-dimethylpyridine Preparation Products And Raw materials

Raw materials

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