Morpholine → 5-Chloro-3-(morpholin-4-yl)methyl-7-nitro-2-phenyl-1H-indole
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([N+:11]([O-:13])=[O:12])[CH:10]=1)[NH:7][C:6]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[C:5]2[CH:20]=O.[NH:22]1[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([N+:11]([O-:13])=[O:12])[CH:10]=1)[NH:7][C:6]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)=[C:5]2[CH2:20][N:22]1[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1Komponenten
3
Versuchsvorschrift
5-Chloro-3-formyl-7-nitro-2-phenyl-1H-indole prepared in Step A of Preparation 43 and morpholine were reacted according to the same procedure as Step B of Preparation 43 to give the title compound.
Aufarbeitung
- customwere reacted
- customaccording to the same procedure as Step B of Preparation 43
Quellen und Nachweise
- ORD-Eintrag
- ord-d7bf6fb4dc1d4154a8cfe6c61d10d377
- Quelldatensatz
- uspto-grants-2015_04
- Patentnummer
- US09000028B2
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