O-Methylhydroxylamine hydrochloride → HCID 86608313, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([N:11]2[CH2:16][CH2:15][CH:14]([NH:17][C:18]([C:20]3[NH:21][C:22]([CH3:27])=[C:23]([Cl:26])[C:24]=3[Cl:25])=[O:19])[CH2:13][CH2:12]2)[N:10]=1)[C:5](O)=[O:6].Cl.[O:29]([NH2:31])[CH3:30]>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([N:11]2[CH2:12][CH2:13][CH:14]([NH:17][C:18]([C:20]3[NH:21][C:22]([CH3:27])=[C:23]([Cl:26])[C:24]=3[Cl:25])=[O:19])[CH2:15][CH2:16]2)[N:10]=1)[C:5]([NH:31][O:29][CH3:30])=[O:6]Komponenten
3
Versuchsvorschrift
The title compound was synthesised by an analogous method to Example 45 starting from 2-chloro-6-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)isonicotinic acid (Example 153) and methoxylamine hydrochloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-0d9ece13e083470fae47798eb6a35574
- Quelldatensatz
- uspto-grants-2010_05
- Patentnummer
- US07709503B2
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