Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11](=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:6]=[C:5]2[CH2:19][C@H:20]1CC[CH2:22][N:21]1[CH3:25].BrC1C=C2C(=CC=1)NC=C2C[C@H]1CCCN1C>>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11](=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:6]=[C:5]2[CH2:19][CH2:20][N:21]([CH3:22])[CH3:25]Participants
3
Procedure
(R)-5-Bromo-3-[(N-methylpyrrolidin-2-yl)methyl]-1-benzoylindole: (76%), from (R)-5-Bromo-3-[(N-methylpyrrolidin-2-yl)methyl]-1H-indole (Example 3d).
Sources & evidence
- ORD record
- ord-67b62456c2b34548a4107df3a06c8518
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998438
Linked notes
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