Acetyl chloride → N-{[3-(2-{[(1-methylethyl)sulfonyl]amino}-2,3-dihydro-1H-inden-5-yl)phenyl]methyl}acetamide
Reaktionsgleichung
[NH2:1][CH2:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:10]=[C:11]3[C:15](=[CH:16][CH:17]=2)[CH2:14][CH:13]([NH:18][S:19]([CH:22]([CH3:24])[CH3:23])(=[O:21])=[O:20])[CH2:12]3)[CH:6]=[CH:7][CH:8]=1.[C:25](Cl)(=[O:27])[CH3:26]>>[CH3:23][CH:22]([S:19]([NH:18][CH:13]1[CH2:12][C:11]2[C:15](=[CH:16][CH:17]=[C:9]([C:5]3[CH:4]=[C:3]([CH2:2][NH:1][C:25](=[O:27])[CH3:26])[CH:8]=[CH:7][CH:6]=3)[CH:10]=2)[CH2:14]1)(=[O:21])=[O:20])[CH3:24]Komponenten
3
Versuchsvorschrift
The title compound was prepared from N-{5-[3-(aminomethyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamide and acetyl chloride in a similar manner to Example 12.
Quellen und Nachweise
- ORD-Eintrag
- ord-d9589a36d332401ea4fed57d7b3c209b
- Quelldatensatz
- uspto-grants-2010_06