N-(2-acetyl-4,6-dimethylphenyl)-3-(((4-chloro-3-methyl-5-isoxazolyl)amino)sulfonyl)-2-thiophenecarboxamide → 3-(((4-Chloro-3-methyl-5-isoxazolyl)amino)sulfonyl)-N-(2-isobutyryl-4,6-dimethylphenyl)-2-thiophenecarboxamide
Reaktionsgleichung
C(C1C=C(C)C=C(C)C=1N[C:13]([C:15]1[S:16][CH:17]=[CH:18][C:19]=1[S:20]([NH:23][C:24]1[O:28][N:27]=[C:26]([CH3:29])[C:25]=1[Cl:30])(=[O:22])=[O:21])=[O:14])(=O)C.[NH2:31][C:32]1[C:37]([CH3:38])=[CH:36][C:35]([CH3:39])=[CH:34][C:33]=1[C:40](=[O:44])[CH:41]([CH3:43])[CH3:42]>>[Cl:30][C:25]1[C:26]([CH3:29])=[N:27][O:28][C:24]=1[NH:23][S:20]([C:19]1[CH:18]=[CH:17][S:16][C:15]=1[C:13]([NH:31][C:32]1[C:37]([CH3:38])=[CH:36][C:35]([CH3:39])=[CH:34][C:33]=1[C:40](=[O:44])[CH:41]([CH3:42])[CH3:43])=[O:14])(=[O:21])=[O:22]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
3-(((4-Chloro-3-methyl-5-isoxazolyl)amino)sulfonyl)-N-(2-isobutyryl-4,6-dimethylphenyl)-2-thiophenecarboxamide was synthesized in the same fashion as for N-(2-acetyl-4,6-dimethylphenyl)-3-(((4-chloro-3-methyl-5-isoxazolyl)amino)sulfonyl)-2-thiophenecarboxamide (Example 39) except that 2′-amino-3′,5′-dimethyl-2-methylpropiophenone was used instead of 2′-amino-3′,5′-dimethylacetophenone.
Quellen und Nachweise
- ORD-Eintrag
- ord-fe6a3f2afe324653ac40e011f946af2e
- Quelldatensatz
- uspto-grants-2004_01
- Patentnummer
- US06683103B2
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