2-CYANO-3-METHOXYPYRIDINE
2-CYANO-3-METHOXYPYRIDINE Basic information
- Product Name:
- 2-CYANO-3-METHOXYPYRIDINE
- Synonyms:
-
- 3-METHOXYPICOLINONITRILE
- 3-METHOXY-PYRIDINE-2-CARBONITRILE
- 3-Methoxy-2-Pyridinecarbonitrile
- 2-CYANO-3-METHOXYPYRIDINE
- 2-Pyridinecarbonitrile, 3-methoxy-
- 2-CYANO-3-METHOXYPYRIDINE ISO 9001:2015 REACH
- CAS:
- 24059-89-0
- MF:
- C7H6N2O
- MW:
- 134.14
- EINECS:
- 1592732-453-0
- Mol File:
- 24059-89-0.mol
2-CYANO-3-METHOXYPYRIDINE Chemical Properties
- Melting point:
- 111-112℃ (ethyl acetate )
- Boiling point:
- 289.8±20.0℃ (760 Torr)
- Density
- 1.16±0.1 g/cm3 (20 ºC 760 Torr)
- Flash point:
- 129.1±21.8℃
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- -4?+-.0.10(Predicted)
- Appearance
- White to off-white Solid
Safety Information
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2933399990
2-CYANO-3-METHOXYPYRIDINE Usage And Synthesis
Synthesis
124-41-4
38180-46-0
24059-89-0
Under nitrogen protection, sodium methanolate (0.41 g, 7.5 mmol) was dissolved in a 25 mL round bottom flask containing 10 mL of anhydrous N,N-dimethylformamide and the mixture was cooled to 4 °C using an ice water bath. Subsequently, 3-chloro-2-cyanopyridine (1.01 g, 7.2 mmol) was added to the reaction system, the ice-water bath was removed, and the reaction system was allowed to slowly warm up to 25 °C. After the reaction was carried out for 2 hours, the solvent was removed by vacuum concentration. Ethyl acetate was added to the concentrated residue and filtered to remove the insoluble precipitate. The filtrate was further concentrated on a rotary evaporator to afford the target product 2-cyano-3-methoxypyridine as a white solid (0.88 g, 88% yield), which could be used in subsequent reactions without further purification. The structure of the product was confirmed by 1H-NMR (CDCl3): δ 8.22 (dd, J = 7.4 and 1.6 Hz, 1H), 7.90 (dd, J = 7.5 and 7.3 Hz, 1H), 7.73 (dd, J = 7.73 and 1.6 Hz, 1H), 3.92 (s, 3H). Mass spectral analysis (ESI+) showed m/z (M + H)+ = 135.
References
[1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 5352 - 5359
[2] Patent: WO2015/187934, 2015, A1. Location in patent: Paragraph 0205
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