2-(4-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine → 2-(7-fluoro-4-methoxy-1-methyl-5-phenyl-1H-indol-3-yl)-N,N-dimethylethanamine
Reaction equation
C(OC1C(F)=CC=C2C=1C(CCN(C)C)=CN2)C1C=CC=CC=1.[F:24][C:25]1[CH:26]=[C:27]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[C:28]([O:41][CH3:42])=[C:29]2[C:33]=1[N:32]([CH3:34])[CH:31]=[C:30]2[CH2:35][C:36]([N:38]([CH3:40])[CH3:39])=O>>[F:24][C:25]1[CH:26]=[C:27]([C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=2)[C:28]([O:41][CH3:42])=[C:29]2[C:33]=1[N:32]([CH3:34])[CH:31]=[C:30]2[CH2:35][CH2:36][N:38]([CH3:39])[CH3:40]Participants
3
Procedure
Following the procedure used to prepare compound 1-7a (step 6 scheme 1), compound 8-12 gave compound 8-13
Sources & evidence
- ORD record
- ord-be86a368de764e148b8b7376800c896b
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912220B2
Reaction notes
Loading…