2-(Bromomethyl)-6-methylpyridine → 5-(4-chlorophenyl)-N-((6-methylpyridin-2-yl)methyl)-N-(4-(piperazin-1-yl)phenyl)furan-2-carboxamide
Reaktionsgleichung
Cc1cccc(CBr)n1.CC(C)(C)OC(=O)N1CCN(c2ccc(NC(=O)c3ccc(-c4ccc(Cl)cc4)o3)cc2)CC1>O=S(=O)(O)O.CC(C)(C)[O-].[Na+].CN(C)C=O.CN(C)C=O.CN(C)C=O.COCCOCCOC>CC(C)(C)OC(=O)N1CCN(c2ccc(NC(=O)c3ccc(-c4ccc(Cl)cc4)o3)cc2)CC1.CC(C)(C)OC(=O)N1CCN(c2ccc(NC(=O)c3ccc(-c4ccc(Cl)cc4)o3)cc2)CC1.Cc1cccc(CN(C(=O)c2ccc(-c3ccc(Cl)cc3)o2)c2ccc(N3CCNCC3)cc2)n1Komponenten
8
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- 23 °C
Aufarbeitung
- additionquenched by addition of saturated aqueous NaHCO3 (2 uL) and diluted with water (1 uL) and DMSO (2 uL)
- additionquenched by addition of saturated aqueous NaHCO3 (2 uL) and diluted with water (1 uL) and DMSO (2 uL)
- additionquenched by addition of saturated aqueous NaHCO3 (2 uL) and diluted with water (1 uL) and DMSO (2 uL)
- additionThe reactions were further diluted to 10 mM using DMSO.
Quellen und Nachweise
- ORD-Eintrag
- ord-226520702b6343029ef1c9a18f126ea0
- Quelldatensatz
- Cernak miniaturized N-alkylation with BOC deprotection
- Originallink
- Quelle ansehen
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