6-bromo-7-methoxy-1H-indole → 3-(7-Methoxy-1H-indol-6-yl)-3-phenyl-acrylic acid ethyl ester
Reaction equation
Br[C:2]1[C:10]([O:11][CH3:12])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.[CH2:13]([O:15][C:16](=[O:36])[CH:17]=[C:18](C1C(OC)=CC=C2C=1C=CN2)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:14]>>[CH2:13]([O:15][C:16](=[O:36])[CH:17]=[C:18]([C:2]1[C:10]([O:11][CH3:12])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:14]Participants
3
Procedure
3-(7-Methoxy-1H-indol-6-yl)-3-phenyl-acrylic acid ethyl ester CXXXVIII was prepared from 6-bromo-7-methoxy-1H-indole using the procedure described above for preparation of 3-(5-Methoxy-1H-Indol-4-yl)-3-phenyl-acrylic acid ethyl ester XLVIII (Example 12).
Sources & evidence
- ORD record
- ord-df65aa2b0cbf470cbae372244ab8ed04
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446118B2
Reaction notes
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