3-Fluoro-4-(3-cyano-1-pyrrolyl)nitrobenzene → 5-Amino-2-(3-cyano-1-pyrrolyl)fluorobenzene
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]([N+:15]([O-])=O)[CH:5]=[CH:6][C:7]=1[N:8]1[CH:12]=[CH:11][C:10]([C:13]#[N:14])=[CH:9]1>CO.[Pd]>[NH2:15][C:4]1[CH:5]=[CH:6][C:7]([N:8]2[CH:12]=[CH:11][C:10]([C:13]#[N:14])=[CH:9]2)=[C:2]([F:1])[CH:3]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
3-Fluoro-4-(3-cyano-1-pyrrolyl)nitrobenzene (5.3 g, 22.9 mmnol) was dissolved in hot MeOH (250 ml) and palladium catalyst (10% on charcoal, 700 mg) added under a nitrogen atmosphere. The mixture was cooled and hydrogenated at atmospheric pressure for 3.5 hours. After filtration through celite, the solution was evaporated to dryness to give title product in sufficent purity for the next stage (4.6 g).
Aufarbeitung
- temperatureThe mixture was cooled
- filtrationAfter filtration through celite
- customthe solution was evaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-312b9797beda4aba96ca2a5a0f066241
- Quelldatensatz
- uspto-grants-2003_09
- Patentnummer
- US06617339B1
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