Dimethyl-(4-piperazin-1-YL-phenyl)-amine → [4-(4-Dimethylamino-phenyl)-piperazin-1-yl]-(4-methanesulfonyl-biphenyl-2-yl)-methanone
Reaction equation
[CH3:1][N:2]([CH3:15])[C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[CH:5][CH:4]=1.[CH3:16][S:17]([C:20]1[CH:21]=[C:22]([C:32](O)=[O:33])[C:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[CH:24][CH:25]=1)(=[O:19])=[O:18]>>[CH3:1][N:2]([CH3:15])[C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:14][CH2:13][N:12]([C:32]([C:22]3[CH:21]=[C:20]([S:17]([CH3:16])(=[O:19])=[O:18])[CH:25]=[CH:24][C:23]=3[C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)=[O:33])[CH2:11][CH2:10]2)=[CH:7][CH:8]=1Participants
3
Procedure
The tide compound was prepared according to the procedure E described for Example 9 from Dimethyl-(4-piperazin-1-yl-phenyl)-amine [91703-23-0] and 4-Methanesulfonyl-biphenyl-2-carboxylic acid (Example V). MS (ISP): 464.3 MH+.
Workup
- customThe tide compound was prepared
Sources & evidence
- ORD record
- ord-b871b386867045bcb3567741d626317d
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07462617B2
Reaction notes
Loading…