Stannous Chloride → 2-Bromo-5-(4-chloro-phenyl)-pyridin-3-ylamine
Reaktionsgleichung
[Br:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=2)=[CH:4][N:3]=1.[Sn](Cl)Cl.C([O-])(O)=O.[Na+]>CCOC(C)=O>[Br:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([C:11]2[CH:12]=[CH:13][C:14]([Cl:17])=[CH:15][CH:16]=2)=[CH:4][N:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 5.60 g (17.9 mmol) 2-bromo-5-(4-chloro-phenyl)-3-nitro-pyridine, 20.3 g (90.0 mmol) tin(II)-chloride and 18.9 g (225 mmol) NaHCO3 in 300 mL EtOAc is refluxed for 30 h. After filtration the solvent is eliminated i.vac. The residue is triturated with DCM and after filtration the filter residue is dried in the air.
Aufarbeitung
- filtrationAfter filtration the solvent
- customThe residue is triturated with DCM
- filtrationafter filtration the filter residue
- customis dried in the air
Quellen und Nachweise
- ORD-Eintrag
- ord-42d186145eb540ad80ecea9f5e9ad76f
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07452911B2
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