O-(4-nitrobenzyl)hydroxylamine → 5-({[3-({[(4-nitrobenzyl)oxy]imino}methyl)benzyl][(1S)-1,2,3,4-tetrahydro-1-naphthalenyl]amino}carbonyl)-1,2,4-benzenetricarboxylic Acid
Reaktionsgleichung
[CH:1]([C:3]1[CH:4]=[C:5]([CH:35]=[CH:36][CH:37]=1)[CH2:6][N:7]([C@@H:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:28][CH2:27][CH2:26]1)[C:8]([C:10]1[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[C:13]([C:19]([OH:21])=[O:20])=[CH:12][C:11]=1[C:22]([OH:24])=[O:23])=[O:9])=O.[N+:38]([C:41]1[CH:49]=[CH:48][C:44]([CH2:45][O:46][NH2:47])=[CH:43][CH:42]=1)([O-:40])=[O:39]>>[N+:38]([C:41]1[CH:42]=[CH:43][C:44]([CH2:45][O:46][N:47]=[CH:1][C:3]2[CH:4]=[C:5]([CH:35]=[CH:36][CH:37]=2)[CH2:6][N:7]([C@@H:25]2[C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[CH2:28][CH2:27][CH2:26]2)[C:8]([C:10]2[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[C:13]([C:19]([OH:21])=[O:20])=[CH:12][C:11]=2[C:22]([OH:24])=[O:23])=[O:9])=[CH:48][CH:49]=1)([O-:40])=[O:39]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The product from Example 76E and O-(4-nitrobenzyl)hydroxylamine were processed as described in Example 76F to provide the title compound.