Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Pyridine derivatives >  2-Amino-6-methoxy-3-nitropyridine

2-Amino-6-methoxy-3-nitropyridine

Basic information Safety Supplier Related

2-Amino-6-methoxy-3-nitropyridine Basic information

Product Name:
2-Amino-6-methoxy-3-nitropyridine
Synonyms:
  • 6-Methoxy-3-nitro-pyridin-2-ylamine
  • 2-Amino-6-methoxy-3-nitropyrid
  • 2-AMINO-3-NITRO-6-METHOXYLPYRIDINE
  • 2-Amino-6-methoxy-3-nitropyridine ,98%
  • TENA-001
  • 6-METHOXY-3-NITRO-2-PYRIDINYLAMINE
  • 6-METHOXY-3-NITROPYRIDIN-2-AMINE
  • 2-PYRIDINAMINE, 6-METHOXY-3-NITRO-
CAS:
73896-36-3
MF:
C6H7N3O3
MW:
169.14
EINECS:
616-028-7
Product Categories:
  • Pyridine
  • Pyridine series
  • Amines
  • Pyridines
  • Pyridines derivates
Mol File:
73896-36-3.mol
More
Less

2-Amino-6-methoxy-3-nitropyridine Chemical Properties

Melting point:
171-172°C
Boiling point:
338.5±37.0 °C(Predicted)
Density 
1.400±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
solid
pka
0.17±0.50(Predicted)
color 
Yellow
CAS DataBase Reference
73896-36-3(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-36/37/38-43
Safety Statements 
26-36/37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333990
More
Less

2-Amino-6-methoxy-3-nitropyridine Usage And Synthesis

Chemical Properties

Yellow solid

Synthesis

124-41-4

27048-04-0

73896-36-3

1. 7.78 g (0.144 mol) of sodium methanolate was mixed with 50.0 mL of methanol and the mixture was cooled to 15 °C. 2. 25.0 g (0.144 mol) of 2-amino-6-chloro-3-nitropyridine was slowly added to the above solution while maintaining 15°C. 3. the reaction mixture was heated to 25°-30°C and stirred continuously at this temperature for 4-5 hours. 4. The progress of the reaction was monitored by thin layer chromatography (TLC). 5. Upon completion of the reaction, the reaction mixture was slowly poured into water to precipitate the product. 6. The precipitate was collected by filtration and washed with cold water. 7. After drying, 21.0 g of 2-amino-3-nitro-6-methoxypyridine was obtained in 86.5% yield and 99.0% purity by HPLC. 8. 8. The melting point of the product was 167°-169°C. 9. 9. 1H-NMR (CDCl3) data: δ 3.89 ppm (single peak, 3H, OCH3), 6.14-6.16 ppm (twin peaks, 1H), 8.24-8.27 ppm (twin peaks, 1H), 8.16 ppm (single peak, 2H, -NH2).

References

[1] Patent: US2006/80790, 2006, A1. Location in patent: Page/Page column 3
[2] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 19 - 32
[3] Journal of Medicinal Chemistry, 1997, vol. 40, # 12, p. 1808 - 1819
[4] Patent: WO2014/57415, 2014, A2. Location in patent: Page/Page column 47

2-Amino-6-methoxy-3-nitropyridineSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com