Indole → HCID 68486868, compound
Reaction equation
[CH:1]1[C:14]2[C:5](=[N:6][CH:7]=[C:8]3[C:13]=2[CH:12]=[CH:11][CH:10]=[CH:9]3)[CH:4]=[CH:3][CH:2]=1.[CH3:15][CH:16]([CH2:20][CH2:21][CH3:22])[C:17](Cl)=[O:18].[NH:23]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[CH:25]=[CH:24]1>>[NH:23]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[C:25]([CH:7]2[C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:14]3[CH:1]=[CH:2][CH:3]=[CH:4][C:5]=3[N:6]2[C:17](=[O:18])[CH:16]([CH3:15])[CH2:20][CH2:21][CH3:22])=[CH:24]1Participants
4
Procedure
1-[6-(1H-Indol-3-yl)-6H-phenanthridin-5-yl]-2-methyl-pentan-1-one was prepared from phenanthridine, 2-methylvaleryl chloride, and indole according to GP 2.
Sources & evidence
- ORD record
- ord-1b21bd84920a4ae68cb2130534c4c57f
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07276606B2
Reaction notes
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