Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:12][CH3:13])[CH:11]=1)[C:6]([NH2:8])=[O:7].[Cl:14][C:15]([Cl:19])([CH3:18])[CH:16]=O.[NH:20]1[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[N:20]1([CH:16]([NH:8][C:6](=[O:7])[C:5]2[CH:9]=[C:10]([O:12][CH3:13])[CH:11]=[C:3]([O:2][CH3:1])[CH:4]=2)[C:15]([Cl:19])([Cl:14])[CH3:18])[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1Komponenten
5
Versuchsvorschrift
A suspension of 3,5-dimethoxybenzamide, 2,2-dichloropropionaldehyde, benzotriazole, and p-toluenesulfonic acid was processed as described in Example 53A to provide the desired product.
Quellen und Nachweise
- ORD-Eintrag
- ord-36adb48f7d7c4e809e838f03eff1498e
- Quelldatensatz
- uspto-grants-2003_11
- Patentnummer
- US06645968B2
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