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5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL

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5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL Basic information

Product Name:
5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL
Synonyms:
  • 5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL
  • 5-AMINO-2-METHOXY-3-PICOLINE HCL
  • 5-AMINO-2-METHOXY-3-PICOLINE HYDROCHLORIDE
  • 3-Amino-6-methoxy-5-methylpyridine
  • 6-methoxy-5-methylpyridin-3-amine
  • 6-Methoxy-5-methyl-3-pyridinamine
  • 2-methoxy-3-methyl-5-aminopyridine
  • 3-Amino-6-methoxy-5-methylpyridine 97%
CAS:
867012-70-2
MF:
C7H10N2O
MW:
138.17
Product Categories:
  • Heterocyclic Compounds
Mol File:
867012-70-2.mol
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5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL Chemical Properties

Melting point:
53-57°C
Boiling point:
268℃
Density 
1.103
Flash point:
116℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
solid
pka
4.62±0.20(Predicted)
Appearance
Pale purple to purple Powder
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
2933399990
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5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL Usage And Synthesis

Synthesis

89694-10-0

867012-70-2

General procedure for the synthesis of 3-amino-6-methoxy-5-methylpyridine from 2-methoxy-5-nitro-3-methylpyridine: (1c) 6-methoxy-5-methyl-3-pyridinamine [Eq. 10]; 2-methoxy-3-methyl-5-nitro-pyridine (1.63 g, 9.71 mmol) was dissolved in methanol (50 mL), 10% Pd/C catalyst was added (50% water content, 800 mg) and the reaction was stirred under hydrogen atmosphere for 2 h 10 min. Upon completion of the reaction, it was filtered through diatomaceous earth and the solvent was evaporated to afford 3-amino-6-methoxy-5-methylpyridine (1.25 g, 9.0 mmol, 93% yield) as a blue oil.1H NMR (400 MHz, DMSO-d6) δ ppm: 2.03 (3H, s), 3.73 (3H, s), 4.62 (2H, s), and 6.83-6.86 (1H, m), 7.31-7.34 (1H, m).

References

[1] Patent: WO2005/103049, 2005, A1. Location in patent: Page/Page column 63-64
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3056 - 3062

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