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Methyl iodide → 6-Amino-4-methoxy-2-methylnicotinonitrile

HRID 928387
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 928387
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([C:9]#[N:10])=[C:4]([O-:11])[CH:3]=1.[Na+].[C:13]([O-])([O-])=O.[K+].[K+].CI.C([O-])(O)=O.[Na+]>CN(C=O)C>[NH2:1][C:2]1[CH:3]=[C:4]([O:11][CH3:13])[C:5]([C:9]#[N:10])=[C:6]([CH3:8])[N:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 516892Sodium BicarbonateHCID 58081220Sodium 6-amino-3-cyano-2-methylpyridin-4-olate

Produkt 1

HCID 667237286-Amino-4-methoxy-2-methylnicotinonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a mixture of sodium 6-amino-3-cyano-2-methylpyridin-4-olate (500 mg, 2.92 mmol, prepared in analogy to WO2001062233A2 and isolated as sodium salt), and K2CO3 (808 mg, 5.84 mmol) in DMF (1 ml) was added MeI (0.200 ml, 3.21 mmol), and the reaction mixture was stirred at it for 9 d. Saturated NaHCO3 (50 ml) was added and the mixture was extracted with EA (4×20 ml). The combined organic extracts were diluted with additional DCM and MeOH until homogeneous, dried over Na2SO4, filtered and concentrated. The crude product was recrystallized from refluxing MeOH-DCM to afford the title compound. 1H-NMR (DMSO-d6, 400 MHz): 2.34 (s, 3H), 3.82 (s, 3H), 5.91 (s, 1H), 6.83 (br, s, 2H); LCMS RtM=1.11 min, [M+H]+=164.2.

Aufarbeitung

  1. extractionthe mixture was extracted with EA (4×20 ml)
  2. additionThe combined organic extracts were diluted with additional DCM and MeOH until homogeneous,
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was recrystallized
  7. temperaturefrom refluxing MeOH-DCM

Quellen und Nachweise

ORD-Eintrag
ord-a063049e807e44a6947682d2b269d4ee
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09290485B2

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