Sodium Methoxide → HCID 89691264, Verbindung
Reaktionsgleichung
Cl.[CH:2]1([C:5]2[N:9]([CH3:10])[C:8]3[CH:11]=[C:12]([N:15]4[CH:20]=[CH:19][C:18]([O:21][CH2:22][C:23](=[NH:25])[NH2:24])=[CH:17][C:16]4=[O:26])[CH:13]=[CH:14][C:7]=3[N:6]=2)[CH2:4][CH2:3]1.F[P-](F)(F)(F)(F)F.[Cl:34][C:35](=[CH:40]N(C)C)[CH:36]=[N+](C)C.C[O-].[Na+]>CO>[Cl:34][C:35]1[CH:36]=[N:25][C:23]([CH2:22][O:21][C:18]2[CH:19]=[CH:20][N:15]([C:12]3[CH:13]=[CH:14][C:7]4[N:6]=[C:5]([CH:2]5[CH2:4][CH2:3]5)[N:9]([CH3:10])[C:8]=4[CH:11]=3)[C:16](=[O:26])[CH:17]=2)=[N:24][CH:40]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2-((1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)-2-oxo-1,2-dihydropyridin-4-yl)oxy)ethanimidamide hydrochloride (100 mg), 2-chloro-3-(dimethylamino)-N,N-dimethylprop-2-en-1-iminium hexafluorophosphate (0.82 ml), sodium methoxide (43.3 mg) and MeOH (10 ml) was stirred at room temperature for 1 h. The mixture was concentrated, and the residue was partitioned between EtOAc and water. The extract was washed with brine, dried over MgSO4, concentrated and purified by NH silica gel column chromatography (hexane/EtOAc) to give the title compound (56 mg) as a white solid.
Aufarbeitung
- concentrationThe mixture was concentrated
- customthe residue was partitioned between EtOAc and water
- washThe extract was washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated
- custompurified by NH silica gel column chromatography (hexane/EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-64f982d5672947d69216678564675f89
- Quelldatensatz
- uspto-grants-2016_06
- Patentnummer
- US09365540B2
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