ChemicalBook--->CAS DataBase List--->53554-20-4

53554-20-4

53554-20-4 Structure

53554-20-4 Structure
IdentificationBack Directory
[Name]

6-AMino-2-chloronicotinonitrile
[CAS]

53554-20-4
[Synonyms]

6-AMino-2-chloronicotinonitrile
6-Amino-2-chloro-3-pyridinecarbonitrile
6-amino-2-chloropyridine-3-carbonitrile
3-Pyridinecarbonitrile, 6-amino-2-chloro-
[Molecular Formula]

C6H4ClN3
[MDL Number]

MFCD18802573
[MOL File]

53554-20-4.mol
[Molecular Weight]

153.57
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

6-AMino-2-chloronicotinonitrile(53554-20-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ZINC CYANIDE

557-21-1

6-Chloro-5-iodopyridin-2-aMine

1221398-11-3

6-AMino-2-chloronicotinonitrile

53554-20-4

6-Chloro-5-iodopyridin-2-amine (4.00 g, 15.7 mmol) and zinc cyanide (0.997 g, 8.50 mmol) were dissolved in 15 mL of N,N-dimethylformamide under argon protection. Subsequently, zinc cyanide was added, and the mixture was vigorously stirred and purged with a stream of argon for 5 min. Next, tris(dibenzylideneacetone)dipalladium(0) (0.642 g, 0.701 mmol) and 1,1'-bis(diphenylphosphino)ferrocene (0.784 g, 1.42 mmol) were added, and the reaction mixture was stirred for 10 min at 120 °C. After completion of the reaction, it was extracted with ethyl acetate and aqueous half-saturated sodium bicarbonate, and the organic phase was concentrated by filtration through silica gel. Finally, purification by silica gel column chromatography (elution gradient: cyclohexane/ethyl acetate 100/0→50/50) afforded the target product 6-amino-2-chlorocyanopyridine in a yield of 1.60 g and 66%. Mass spectrum (ESI+): m/z = 154 [M + H]+.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 5, p. 1697 - 1700
[2] Patent: US2018/37594, 2018, A1. Location in patent: Paragraph 0344-0347
[3] European Journal of Medicinal Chemistry, 2014, vol. 84, p. 404 - 416
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