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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 98%;2-cyano-2-Methoxy-1,2-dihydropyridine-4-carboxylic acid;2-Methoxy-4-Pyridinecarbonitrile;4-Pyridinecarbonitrile, 2-methoxy-;2-Methoxyisonicotinonitrile 98%;2-METHOXYISONICOTINONITRILE;4-Cyano-2-methoxypyridine
CAS:72716-86-0
MF:C7H6N2O
MW:134.14
EINECS:
Product Categories:blocks;Carboxes;Pyridines
Mol File:72716-86-0.mol
4-Cyano-2-methoxypyridine Structure
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
pka0.04±0.10(Predicted)
color White
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2933399990
MSDS Information
4-Cyano-2-methoxypyridine Usage And Synthesis
Uses4-Cyano-2-methoxypyridine is a reagent used in the synthesis of hydroxypyridone derivatives which are bioisosters of capsain.
Synthesis
2-Chloro-4-cyanopyridine

33252-30-1

Sodium Methoxide

124-41-4

4-CYANO-2-METHOXYPYRIDINE

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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