Indole → HCID 68492242, 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.[C:15](Cl)(=[O:24])[CH2:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.[NH:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27]1>>[NH:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[C:28]([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:15](=[O:24])[CH2:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:27]1Participants
4
Procedure
1-[6-(1H-Indol-3-yl)-6H-phenanthridin-5-yl]-3-phenyl-propan-1-one was prepared from phenanthridine, hydrocinnamoyl chloride, and indole according to GP 2.
Sources & evidence
- ORD record
- ord-4619659c7c224d5488c64262060b461a
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07276606B2
Reaction notes
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