3,5-Dichloro-2-cyanopyridine → 3-Chloro-5-methoxypicolinonitrile

HRID 340218

Reaktionsgleichung

Reaktionsgleichung von HRID 340218
[Cl:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][CH:5]=[C:6](Cl)[CH:7]=1.[CH3:11][O-:12].[Na+]>CN(C)C=O.C(OCC)(=O)C.O>[Cl:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][CH:5]=[C:6]([O:12][CH3:11])[CH:7]=1

Komponenten

6

Edukt 2

HCID 27696993,5-Dichloro-2-cyanopyridineHCID 10942334Sodium Methoxide

Produkt 1

HCID 187968643-Chloro-5-methoxypicolinonitrile

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

To a solution of 3,5-dichloropicolinonitrile (1.0 eq.) in dimethyl formamide (DMF) (0.5 M) was added sodium methoxide (1.5 eq.) and heated to 75° C. After stirring for 14 hours, the reaction was diluted with ethyl acetate and water. The organic layer was washed with saturated aqueous NaHCO3 three times, water twice, dried over anhydrous MgSO4, and concentrated en vacuo. The crude residue was purified by a COMBIFLASH® system (ISCO) using 15% ethyl acetate in hexane to give a mixture of two methoxy regioisomers, one of which was the desired product. The mixture was carried onto the next step without further purification.

Aufarbeitung

  1. washThe organic layer was washed with saturated aqueous NaHCO3 three times, water twice
  2. dry with materialdried over anhydrous MgSO4
  3. concentrationconcentrated en vacuo
  4. customThe crude residue was purified by a COMBIFLASH® system (ISCO)
  5. customto give
  6. additiona mixture of two methoxy regioisomers, one of which

Quellen und Nachweise

ORD-Eintrag
ord-644b96ca644b477a93e2eaf644a3f724
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08895577B2

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