Hydrogen Bromide → 4-Chloro-3-iodopyridin-2-amine
Reaktionsgleichung
Br.[Cl:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([NH:9]C(=O)OC(C)(C)C)[C:4]=1[I:17].[OH-].[Na+]>O>[Cl:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([NH2:9])[C:4]=1[I:17]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of aqueous HBr (48%, 10 mL, 13.26 mmol) was added to tert-butyl (4-chloro-3-iodopyridin-2-yl)carbamate (4.7 g, 13.26 mmol) and the suspension was stirred at RT for 3 h. The reaction mixture was diluted with water (40 ml), basified with 2N NaOH and the resultant suspension was filtered, washed with water (4×1 mL) and dried to afford 4-chloro-3-iodopyridin-2-amine as white solid (3.05 g, 90% yield). MS (ESI) m/z: 254.9 (M+H+).
Aufarbeitung
- filtrationthe resultant suspension was filtered
- washwashed with water (4×1 mL)
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-399d47f5fba5491899c37c1490d9db8f
- Quelldatensatz
- uspto-grants-2013_10
- Patentnummer
- US08569319B2
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