ChemicalBook--->CAS DataBase List--->356783-16-9

356783-16-9

356783-16-9 Structure

356783-16-9 Structure
IdentificationBack Directory
[Name]

3,6-dichloropyrazine-2-carbonitrile
[CAS]

356783-16-9
[Synonyms]

QC-100
Favipiravir Impurity 18
,6-Dichloropyrazine-2-carbonitrile
3,6-dichloropyrazine-2-carbonitrile
3,6-Dichloro-2-pyrazinecarbonitrile
2-Pyrazinecarbonitrile, 3,6-dichloro-
[EINECS(EC#)]

202-303-5
[Molecular Formula]

C5HCl2N3
[MDL Number]

MFCD22199269
[MOL File]

356783-16-9.mol
[Molecular Weight]

173.988
Chemical PropertiesBack Directory
[Melting point ]

93 - 95°C
[Boiling point ]

262.0±35.0℃ (760 Torr)
[density ]

1.60±0.1 g/cm3 (20 ºC 760 Torr)
[Fp ]

112.3±25.9℃
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

-7.43±0.10(Predicted)
[color ]

Pale Yellow to Light Yellow
[Stability:]

Stable under recommended storage conditions., Stable Under Recommended Storage C
[CAS DataBase Reference]

356783-16-9
Safety DataBack Directory
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

3,6-Dichloro-2-pyrazinecarbonitrile is useful in the production of Favipiravir (F103350) a drug that is used for the treatment of advanced Ebola virus infection in a small animal model.
[Synthesis]

2-Pyrazinecarboxamide, 1,4-dioxide

18960-19-5

3,6-dichloropyrazine-2-carbonitrile

356783-16-9

1.46 g of 1,4-dioxopyrazinamide (2) was homogeneously mixed with 5 mL of chlorobenzene and 12.1 g of trichlorophosphorus. The mixture was heated to 50 °C and the reaction was stirred for 50 minutes, followed by warming to 70 °C for 1 hour. Upon completion of the reaction, the mixture was cooled to room temperature, 1.52 g of pyridine was added, and the reaction was continued to 110 °C and maintained for 8 hours. The completion of the reaction was confirmed by TLC monitoring. The reaction mixture was evaporated to dryness under reduced pressure, washed with 5 mL of ice water and subsequently extracted with ethyl acetate (10 mL x 3). The organic phase was combined and washed twice with saturated brine. The organic phase was dried over anhydrous sodium sulfate and filtered, and the filtrate was evaporated to dryness under reduced pressure. Purification by chromatography, separation and vacuum drying gave 1.45 g of light yellow solid 3,6-dichloro-2-cyanopyrazine (3) in 52.55% yield.

[References]

[1] Patent: CN106478528, 2017, A. Location in patent: Paragraph 0033; 0039; 0045
[2] Patent: CN107226794, 2017, A. Location in patent: Paragraph 0039
Spectrum DetailBack Directory
[Spectrum Detail]

3,6-dichloropyrazine-2-carbonitrile(356783-16-9)1HNMR
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