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6-Methoxy-2-methylpyridin-3-amine

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6-Methoxy-2-methylpyridin-3-amine Basic information

Product Name:
6-Methoxy-2-methylpyridin-3-amine
Synonyms:
  • 3-AMINO-6-METHOXY-2-PICOLINE
  • 5-AMINO-2-METHOXY-6-PICOLINE
  • 6-Methoxy-2-methyl-3-pyridylamine
  • 2-Methoxy-5-amino-6-methylpyridine
  • 2-Methyl-6-methoxypyridin-3-amine
  • 3-Amino-6-methoxy-2-methylpyridine 98%
  • 6-Methoxy-2-methyl-3-pyridinamine
  • 6-Methoxy-2-methyl-pyridin-3-ylamine
CAS:
52090-56-9
MF:
C7H10N2O
MW:
138.17
Product Categories:
  • Heterocycle-Pyridine series
  • Pyridine
Mol File:
52090-56-9.mol
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6-Methoxy-2-methylpyridin-3-amine Chemical Properties

Boiling point:
260.0±35.0 °C(Predicted)
Density 
1.103±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
5.05±0.10(Predicted)
Appearance
Light yellow to brown Solid-Liquid Mixture
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Safety Information

HS Code 
2933399990
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6-Methoxy-2-methylpyridin-3-amine Usage And Synthesis

Synthesis

5467-69-6

52090-56-9

6-Methoxy-2-methyl-3-nitropyridine (2 g, 0.012 mol) was used as starting material, which was dissolved in H2O/MeOH (1:1, 40 mL) mixed solvent. Subsequently, NH4Cl (2.2 g, 3.5 eq.) and iron powder (2.3 g, 3.5 eq.) were added to the solution. The reaction mixture was stirred at 80 °C for 16 hours. After completion of the reaction, the iron powder was removed by filtration and the filtrate was washed with MeOH. The MeOH was removed from the filtrate by evaporation, diluted with H2O, and then the aqueous phase was extracted with EtOAc (3 x 50 mL). The organic phases were combined and dried with anhydrous Na2SO4. The desiccant was removed by filtration and the solvent was evaporated to dryness to give 2-methoxy-5-amino-6-methylpyridine (1.35 g, 81% yield) as a brown oil. Its nuclear magnetic resonance hydrogen spectrum (1H NMR, CDCl3) data were as follows: δ 6.9 (d, 1H), 6.4 (d, 1H), 3.8 (s, 3H), 2.33 (s, 3H).

References

[1] Patent: WO2004/62665, 2004, A1. Location in patent: Page/Page column 45
[2] Journal of the Chemical Society, <1954> 2448, 2452,

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