Cyclopentanone → 7-(Cyclopentyl)amino-2-phenyl-1H-indole-5-carboxylic acid ethyl ester
Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([N+:15]([O-])=O)[CH:14]=1)[NH:11][C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[CH:9]2)=[O:5])[CH3:2].[C:24]1(=O)[CH2:28][CH2:27][CH2:26][CH2:25]1>>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([NH:15][CH:24]3[CH2:28][CH2:27][CH2:26][CH2:25]3)[CH:14]=1)[NH:11][C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[CH:9]2)=[O:5])[CH3:2]Komponenten
3
Versuchsvorschrift
2-Phenyl-7-nitro-1H-indole-5-carboxylic acid ethyl ester prepared in Step A and cyclopentanone were reacted according to the same procedure as Example 1 to give the title compound.
Quellen und Nachweise
- ORD-Eintrag
- ord-ac878fd8bd194da98863d9453a1f4c18
- Quelldatensatz
- uspto-grants-2013_05
- Patentnummer