Sodium Methoxide → 1-Methoxy-7-nitroisoquinoline

HRID 2187595Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2187595
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[CH:5]=[CH:4][N:3]=1.[CH3:15][O-:16].[Na+]>CO>[CH3:15][O:16][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[CH:5]=[CH:4][N:3]=1

Komponenten

4

Edukt 2

HCID 10942334Sodium MethoxideHCID 218626571-chloro-7-nitroisoquinoline

Produkt 1

HCID 223970461-Methoxy-7-nitroisoquinolineAusbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a suspension of 1-chloro-7-nitroisoquinoline (670 mg, 3.21 mmol) obtained in Preparation Example 1-5, Step 4 in methanol (100 ml) was added a 1M solution (6.5 ml, 6.5 mmol) of sodium methoxide. The mixture was refluxed under heating for 3 hr and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:acetone=30:1) to give 1-methoxy-7-nitroisoquinoline (530 mg, 81%).

Aufarbeitung

  1. temperatureThe mixture was refluxed
  2. temperatureunder heating for 3 hr
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was dissolved in ethyl acetate
  5. washwashed with saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by silica gel column chromatography (chloroform:acetone=30:1)

Quellen und Nachweise

ORD-Eintrag
ord-dc1dd2b9b3594d3a944af85cf88e6376
Quelldatensatz
uspto-grants-2002_06
Patentnummer
US06410561B1

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