Water → 2-bromo-N-(5-methylpyrazin-2-yl)acetamide
Reaktionsgleichung
[CH3:1][C:2]1[N:3]=[CH:4][C:5]([NH2:8])=[N:6][CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[Br:15][CH2:16][C:17](Br)=[O:18].O>CN(C=O)C>[Br:15][CH2:16][C:17]([NH:8][C:5]1[CH:4]=[N:3][C:2]([CH3:1])=[CH:7][N:6]=1)=[O:18]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a mixture of 5-methyl-pyrazin-2-ylamine and cesium carbonate (11.2 g) dissolved in dry DMF (30 mL) was added by dropwise addition bromoacetylbromide (2.89 g) and the mixture stirred at rt for 2 hours. Water (200 mL) was added and the mixture extracted with ethyl acetate (2×100 mL) and dried over magnesium sulfate. Concentration of the extract to ˜50 mL and addition of isohexane (100 mL) gave the sub-titled compound as a solid (1.64 g).
Aufarbeitung
- extractionthe mixture extracted with ethyl acetate (2×100 mL)
- dry with materialdried over magnesium sulfate
- extractionConcentration of the extract to ˜50 mL and addition of isohexane (100 mL)
Quellen und Nachweise
- ORD-Eintrag
- ord-054691063b1a44ea94dfbd91cf400a74
- Quelldatensatz
- uspto-grants-2012_12
- Patentnummer
- US08329729B2
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