Reaktionsgleichung
[CH:1]1[C:2]2[N:3]([CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:5][N:6]=1.S(=O)(=O)(O)O.[N+:15]([O-])([OH:17])=[O:16].[OH-].[Na+]>C(O)(=O)C>[N+:15]([C:9]1[CH:8]=[CH:7][N:3]2[CH:4]=[CH:5][N:6]=[CH:1][C:2]=12)([O-:17])=[O:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5.5 g of pyrrolo[1,2-a]pyrazine prepared in Preparation Example 1 was dissolved in 10 ml of glacial acetic acid; and to the resulting mixture was added dropwise a mixture of sulfuric acid/nitric acid (15 ml/15 ml) at 0° C. The reaction mixture was stirred at room temperature for 30 minutes, poured into 200 ml of ice-water, and then adjusted to pH 10 with sodium hydroxide solution. The resulting solution was extracted with ethyl acetate (100 ml×3), and concentrated to dryness to obtain 4.3 g of title compound.
Aufarbeitung
- additionand to the resulting mixture was added dropwise
- extractionThe resulting solution was extracted with ethyl acetate (100 ml×3)
- concentrationconcentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-905c6bb533cd4d72b1b7e1b71c45a935
- Quelldatensatz
- uspto-grants-1997_01
- Patentnummer
- US05593984
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