Reaktionsgleichung
CS(O[CH2:6][CH2:7][C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][C:11]=2[CH:12]=1)(=O)=O.[C:25]([NH:29][CH3:30])([CH3:28])([CH3:27])[CH3:26]>>[C:25]([N:29]([CH3:30])[CH2:6][CH2:7][C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][C:11]=2[CH:12]=1)([CH3:28])([CH3:27])[CH3:26]Komponenten
3
Versuchsvorschrift
The product from Example 1C and tert-butyl(methyl)amine were processed as described in Example 1D to provide the titled compound. MS (DCI) m/z 333 (+H)+;
Quellen und Nachweise
- ORD-Eintrag
- ord-917f4bd311514517b9b8281539cfadaf
- Quelldatensatz
- uspto-grants-2009_05
- Patentnummer
- US07538138B2
Verknüpfte Notizen
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