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5-Amino-2-bromo-6-picoline

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5-Amino-2-bromo-6-picoline Basic information

Product Name:
5-Amino-2-bromo-6-picoline
Synonyms:
  • 3-AMINO-6-BROMO-2-METHYLPYRIDINE
  • 3-AMINO-6-BROMO-2-PICOLINE
  • 6-BROMO-2-METHYL-PYRIDIN-3-YLAMINE
  • 6-Bromo-5-amino-2-picoline
  • 6-BROMO-3-AMINO-2-PICOLINE (5-AMINO-2-BROMO-6-PICOLINE)
  • 5-AMINO-2-BROMO-6-PICOLINE (5-AMINO-2-BROMO-6-METHYLPYRIDINE)
  • 3-Pyridinamine, 6-bromo-2-methyl-
  • 2-Bromo-5-amino-6-methylpyridine
CAS:
126325-47-1
MF:
C6H7BrN2
MW:
187.04
EINECS:
251-156-6
Product Categories:
  • Heterocycle-Pyridine series
  • Amino-pyridine series
  • Pyridines
  • Boronic Acid
  • Pyridine
Mol File:
126325-47-1.mol
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5-Amino-2-bromo-6-picoline Chemical Properties

Melting point:
110-111℃
Boiling point:
284.4±35.0 °C(Predicted)
Density 
1.593±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
2.45±0.10(Predicted)
form 
Solid
color 
Off-white
CAS DataBase Reference
126325-47-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-41-37/38-22
Safety Statements 
26-36-39
HS Code 
29333999
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5-Amino-2-bromo-6-picoline Usage And Synthesis

Chemical Properties

crystalline powder

Uses

5-Amino-2-bromo-6-picoline is a useful research intermediate.

Synthesis

22282-96-8

126325-47-1

General procedure for the synthesis of 2-bromo-5-amino-6-methylpyridine from 2-bromo-5-nitro-6-methylpyridine: 6-bromo-2-methyl-3-nitropyridine (XIV) (250 g, 1.15 mol, 1.00 equiv) and NH4Cl (300 g, 5.61 mol, 4.88 equiv) were suspended in a mixture of EtOH (3.50 L) and water ( 150 mL) in a solvent mixture. The suspension was heated to 65 °C under stirring. Subsequently, Fe (130 g, 2.33 mol, 2.02 eq.) and HCl (15.3 g, 419 mmol, 0.36 eq.) were added to the reaction system. The reaction mixture was heated to 80 °C and maintained at this temperature for 3 hours. After completion of the reaction, the mixture was cooled to 25 °C and filtered through a diatomaceous earth plug. The filtrate was concentrated under reduced pressure to give the crude product. The crude product was dissolved in EtOAc (1 L x 3) and washed with brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 6-bromo-2-methylpyridin-3-amine (XV) as a brown solid (373 g, 1.99 mol, 86.7% yield), which could be used in the next reaction without further purification.1H NMR (DMSO-d6, 400 MHz) δ ppm: 6.01 (dd, J = 2.3, 7.9 Hz, 2H). 7.9 Hz, 2H), 7.03 (d, J = 8.2 Hz, 1H); ESIMS m/z: 186.8 ([M + H]+).

References

[1] Patent: WO2017/23993, 2017, A1. Location in patent: Paragraph 0615; 0616
[2] Patent: WO2017/24004, 2017, A1. Location in patent: Paragraph 0610-0611
[3] Patent: WO2017/24025, 2017, A1. Location in patent: Paragraph 0611
[4] Patent: WO2017/24003, 2017, A1. Location in patent: Paragraph 0610; 0611
[5] Patent: US2016/347717, 2016, A1. Location in patent: Paragraph 0593; 0594

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