Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][N:4]=[C:3]2[NH:7][CH:8]=[CH:9][C:2]=12.[N+:10]([O-])([OH:12])=[O:11].C(=O)(O)[O-].[Na+]>O>[N+:10]([C:9]1[C:2]2[C:3](=[N:4][CH:5]=[CH:6][N:1]=2)[NH:7][CH:8]=1)([O-:12])=[O:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
7-Nitro-5H-pyrrolo[2,3-b]pyrazine (5) is prepared by adding 5H-pyrrolo[2,3-b]pyrazine (3) to fuming nitric acid while cooling (e.g. 0° C.). After stirring for one to several hours, water is carefully added and the mixture neutralized with saturated sodium bicarbonate. The solids are collected by filtration and dried to provide 7-nitro-5H-pyrrolo[2,3-b]pyrazine 5.
Aufarbeitung
- custom7-Nitro-5H-pyrrolo[2,3-b]pyrazine (5) is prepared
- additionis carefully added
- filtrationThe solids are collected by filtration
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-154cf4acfdd640b3a18fb50da19058f6
- Quelldatensatz
- uspto-grants-2012_02
- Patentnummer
- US08119637B2
Verknüpfte Notizen
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