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Methyl morpholine oxide → 1-(2,3-Dihydroxypropyl)-7-methoxyquinoxalin-2(1H)-one

HRID 1846999
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1846999
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([N:7]=[CH:8][C:9](=[O:16])[N:10]2CC=C)=[CH:5][CH:4]=1.C[N+]1([O-])CC[O:21]CC1.O1CCCC1.O.[CH3:31][C:32]([CH3:34])=[O:33]>C(OCC)(=O)C.[Os](=O)(=O)(=O)=O>[OH:33][CH:32]([CH2:34][OH:21])[CH2:31][N:10]1[C:11]2[C:6](=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[CH:12]=2)[N:7]=[CH:8][C:9]1=[O:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 82029Methyl morpholine oxideHCID 21553975Acetone water tetrahydrofuranHCID 68810513HCID 68810513, Verbindung

Produkt 1

HCID 867249291-(2,3-Dihydroxypropyl)-7-methoxyquinoxalin-2(1H)-oneAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 30318Osmium TetroxideKatalysator
HCID 8857
Ethyl Acetate
Lösungsmittel

Versuchsvorschrift

7-Methoxy-1-(2-propen-1-yl)quinoxalin-2(1H)-one (synthesized with reference to WO2008/9700; 2.77 g, 12.82 mmol) was dissolved in a mixed solvent (100 ml) of tetrahydrofuran/water/acetone (2:1:2). N-methylmorpholineoxide (3.47 g, 25.64 mmol) was added to this solution under cooling on ice and a 4% aqueous solution of osmium tetroxide (1.6 ml, 0.256 mmol) was subsequently added. The reaction solution was stirred for 2 days while the temperature was raised to room temperature. The reaction solution was diluted with ethyl acetate and washed with saturated sodium bicarbonate water and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to yield 3.16 g (99%) of the title compound in the form of a brown oily product.

Aufarbeitung

  1. temperatureunder cooling on ice
  2. washwashed with saturated sodium bicarbonate water and saturated sodium chloride solution
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customthe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ec7f3d046d9241bca7d8316e11ac9adf
Quelldatensatz
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08952010B2

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