Benzenesulfonamide → 11-[(Phenylsulfonyl)aminocarbonyl]methylthio-2-(quinolin-2-yl)methoxy-6,11-dihydrodibenz[b,e]oxepine
Reaktionsgleichung
[C:1]([CH2:4][S:5][CH:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:10][O:9][C:8]2[CH:17]=[CH:18][C:19]([O:21][CH2:22][C:23]3[CH:32]=[CH:31][C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)=[CH:20][C:7]1=2)([OH:3])=O.[C:33]1([S:39]([NH2:42])(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>>[C:33]1([S:39]([NH:42][C:1]([CH2:4][S:5][CH:6]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[CH2:10][O:9][C:8]3[CH:17]=[CH:18][C:19]([O:21][CH2:22][C:23]4[CH:32]=[CH:31][C:30]5[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=5)[N:24]=4)=[CH:20][C:7]2=3)=[O:3])(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1Komponenten
3
Versuchsvorschrift
11-Carboxymethylthio-2-(quinolin-2-yl)methoxy-6,11-dihydrodibenz[b,e]oxepine and benzensulfonamide were used and reacted in the same manner as in Example 39 to obtain the title compound.
Aufarbeitung
- customreacted in the same manner as in Example 39