Allyl bromide → N-Allyl-N-(2,2,2-trifluoroethyl)-3-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]benzamide
Reaction equation
[C:1]1([CH:7]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][N:13]([C:16]3[CH:17]=[C:18]([CH:27]=[CH:28][CH:29]=3)[C:19]([NH:21][CH2:22][C:23]([F:26])([F:25])[F:24])=[O:20])[CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:36](Br)[CH:37]=[CH2:38]>>[CH2:38]([N:21]([CH2:22][C:23]([F:25])([F:26])[F:24])[C:19](=[O:20])[C:18]1[CH:27]=[CH:28][CH:29]=[C:16]([N:13]2[CH2:12][CH2:11][N:10]([CH2:9][CH2:8][CH:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[CH2:15][CH2:14]2)[CH:17]=1)[CH:37]=[CH2:36]Participants
3
Procedure
The procedure of step (b) of Example 33 was repeated using the compound prepared in step (a) of Example 33, except that allyl bromide was used instead of benzyl bromide. Thus, the title compound was prepared.
Sources & evidence
- ORD record
- ord-1f08d7c13a7d4349a3c901a640a27437
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06777414B1
Reaction notes
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