Water → 2-N-methyl-6-fluoro-1-isoquinolinone

HRID 575553

Reaktionsgleichung

Reaktionsgleichung von HRID 575553
[H-].[Na+].[F:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[C:10](=[O:14])[NH:9][CH:8]=[CH:7]2.[CH3:15]I.O>CN(C=O)C.C(OCC)(=O)C>[F:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[C:10](=[O:14])[N:9]([CH3:15])[CH:8]=[CH:7]2

Komponenten

7

Edukt 4

HCID 962WaterHCID 6328Methyl iodide2×HCID 24758Sodium hydrideHCID 450908026-Fluoroisoquinolin-1(2H)-one

Produkt 1

HCID 693999762-N-methyl-6-fluoro-1-isoquinolinoneAusbeute 107,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel2×

Versuchsvorschrift

Sodium hydride (60% in mineral oil) (211 mg, 5.27 mmol) was added to 6-fluoro-1,2-dihydroisoquinolin-1-one (716 mg, 4.39 mmol) in anhydrous DMF (6 mL) cooled in an ice bath. The mixture was stirred for about 30 min at room temperature and methyl iodide (0.328 mL, 5.27 mmol) was added dropwise. After 1 h, the reaction was judged to be about 60% complete and additional methyl iodide (0.2 mL, 3.2 mmol) was added. After about 1 h, ice and water and ethyl acetate were added to the mixture. After extractive work up with ethyl acetate, the title compound (836 mg) was obtained as a cream solid and carried on without purification.

Aufarbeitung

  1. temperaturecooled in an ice bath
  2. waitAfter 1 h
  3. waitAfter about 1 h

Quellen und Nachweise

ORD-Eintrag
ord-0e5454cf6fb4431a84ed25aa1fe6640b
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09034900B2

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