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4-CYANO-2-METHOXYPYRIDINE

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4-CYANO-2-METHOXYPYRIDINE Basic information

Product Name:
4-CYANO-2-METHOXYPYRIDINE
Synonyms:
  • 4-CYANO-2-METHOXYPYRIDINE
  • 2-METHOXYISONICOTINONITRILE
  • 4-Cyano-2-methoxypyridine 98%
  • 2-cyano-2-Methoxy-1,2-dihydropyridine-4-carboxylic acid
  • 2-Methoxy-4-Pyridinecarbonitrile
  • 4-Pyridinecarbonitrile, 2-methoxy-
  • 2-Methoxyisonicotinonitrile 98%
CAS:
72716-86-0
MF:
C7H6N2O
MW:
134.14
Product Categories:
  • blocks
  • Carboxes
  • Pyridines
Mol File:
72716-86-0.mol
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4-CYANO-2-METHOXYPYRIDINE Chemical Properties

Melting point:
88-92
Boiling point:
207.1±25.0 °C(Predicted)
Density 
1.16±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
pka
0.04±0.10(Predicted)
color 
White
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2933399990
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4-CYANO-2-METHOXYPYRIDINE Usage And Synthesis

Uses

4-Cyano-2-methoxypyridine is a reagent used in the synthesis of hydroxypyridone derivatives which are bioisosters of capsain.

Synthesis

33252-30-1

124-41-4

72716-86-0

General procedure for the synthesis of 4-cyano-2-methoxypyridine from 2-chloro-4-cyanopyridine and sodium methanol: To a solution of 2-chloro-4-cyanopyridine (1.38 g, 10 mmol) in dioxane (10 mL) was added a methanolic solution of sodium methanol (25%, 2.27 g, 10.5 mmol). The reaction mixture was heated to reflux for 5 h, followed by cooling to room temperature and standing overnight in a refrigerator. The precipitate was collected by filtration and washed with methanol. The filtrate was concentrated to about 10 mL and water (100 mL) was added. The precipitate was collected by filtration again and washed with water to give 4-cyano-2-methoxypyridine (1.93 g, 72% yield) as a white solid. Mass spectrum (electrospray positive ion mode) m/z 135 [M + H]+.

References

[1] Journal of Medicinal Chemistry, 2008, vol. 51, # 21, p. 6631 - 6634
[2] Patent: WO2006/9889, 2006, A1. Location in patent: Page/Page column 54
[3] Patent: WO2006/33011, 2006, A1. Location in patent: Page/Page column 28
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 7, p. 2669 - 2684
[5] European Journal of Medicinal Chemistry, 1993, vol. 28, # 7-8, p. 601 - 608

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