Benzyl Bromide → HCID 136393281, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9]C)[CH:6]=[CH:5][C:4]=1[C:11]1[C:19]2[C:14](=[C:15]([C:20]([F:23])([F:22])[F:21])[CH:16]=[CH:17][CH:18]=2)[NH:13][N:12]=1.[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:24]([N:12]1[C:11]([C:4]2[CH:5]=[CH:6][C:7]([OH:9])=[CH:8][C:3]=2[O:2][CH3:1])=[C:19]2[C:14]([C:15]([C:20]([F:23])([F:21])[F:22])=[CH:16][CH:17]=[CH:18]2)=[N:13]1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1Participants
3
Procedure
Prepared according to Example 116 from 3-(2,4-dimethoxyphenyl)-7-(trifluoromethyl)-1H-indazole and benzyl bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-258ca2d6e2644c4bab003cacdfa98eb3
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592363B2
Reaction notes
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