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2-AMINO-5-BROMO-4 6-DIMETHYLPYRIDINE

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2-AMINO-5-BROMO-4 6-DIMETHYLPYRIDINE Basic information

Product Name:
2-AMINO-5-BROMO-4 6-DIMETHYLPYRIDINE
Synonyms:
  • 6-Amino-3-bromo-2,4-iutidine
  • 3-Bromo-2,4-dimethylpyridin-6-amine
  • 2-AMino-4,6-diMethyl-5-broMopyridine
  • 5-BroMo-4,6-diMethylpyridin-2-aMine
  • 5-bromo-4,6-dimethyl-2-pyridinamine
  • 6-Amino-2,4-dimethyl-3-bromopyridine
  • 5-Bromo-4,6-dimethyl-2-pyridinamine, 6-Amino-3-bromo-2,4-lutidine
  • 2-AMino-5-broMo-4,6-diMethylpyridine 97%
CAS:
89856-44-0
MF:
C7H9BrN2
MW:
201.06
EINECS:
626-748-3
Product Categories:
  • Nucleotides
  • Amines
  • Aromatics
  • Bases & Related Reagents
  • Heterocycles
Mol File:
89856-44-0.mol
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2-AMINO-5-BROMO-4 6-DIMETHYLPYRIDINE Chemical Properties

Melting point:
144-148 °C (lit.)
Boiling point:
257.7±35.0 °C(Predicted)
Density 
1.504±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Chloroform, Methanol
form 
Off-White to Pale Beige Solid
pka
5.46±0.48(Predicted)
Appearance
Off-white to yellow Solid
InChIKey
BFRMYMFNSHASRJ-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41-43
Safety Statements 
26-36/37/39
WGK Germany 
3
HS Code 
2933399990
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2-AMINO-5-BROMO-4 6-DIMETHYLPYRIDINE Usage And Synthesis

Chemical Properties

White Powder

Synthesis

5407-87-4

89856-44-0

Example 2: Preparation of 2-amino-5-bromo-4,6-dimethylpyridine (13): 2.00 g (16.32 mmol) of 2-amino-4,6-dimethylpyridine was dissolved in 25 mL of acetonitrile under argon protection and 2.90 g (16.32 mmol) of N-bromosuccinimide was added with stirring. The reaction mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the resulting precipitate was collected by filtration and dried to afford the target product 2-amino-5-bromo-4,6-dimethylpyridine as a white solid in a yield of 2.76 g (84% yield). The structure of the product was confirmed by 1H-NMR (CDCl3) δ 6.22 (s, 1H), 4.39 (br, 2H), 2.48 (s, 3H), 2.25 (s, 3H) and 13C-NMR (CDCl3) δ 156.34, 155.23, 148.64, 112.26, 108.10, 25.10, 23.30.

References

[1] Organic Process Research and Development, 2012, vol. 16, # 1, p. 109 - 116
[2] Patent: WO2011/103536, 2011, A1. Location in patent: Page/Page column 43-44
[3] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 17, p. 5188 - 5201
[4] Pharmacy and Pharmacology Communications, 1999, vol. 5, # 3, p. 233 - 238
[5] Patent: WO2018/108671, 2018, A1. Location in patent: Page/Page column 178; 179

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