HCID 14998775, compound → HCID 14998831, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([N:10]2[CH2:15][CH2:14][N:13]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[C:19]([O:25][CH3:26])[CH:18]=3)[CH:12]([CH2:27][NH2:28])[CH2:11]2)[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.[N:29]1([C:34]2[CH:39]=[CH:38][C:37]([S:40](Cl)(=[O:42])=[O:41])=[CH:36][CH:35]=2)[CH:33]=[CH:32][N:31]=[CH:30]1>>[Br:1][C:2]1[CH:3]=[C:4]([N:10]2[CH2:15][CH2:14][N:13]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[C:19]([O:25][CH3:26])[CH:18]=3)[CH:12]([CH2:27][NH:28][S:40]([C:37]3[CH:38]=[CH:39][C:34]([N:29]4[CH:33]=[CH:32][N:31]=[CH:30]4)=[CH:35][CH:36]=3)(=[O:41])=[O:42])[CH2:11]2)[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1Participants
3
Procedure
In a manner similar to Preparation 3, react 4-(3-bromo-5-methoxyphenyl)-1-[(3,4-dimethoxyphenyl)methyl]-2-piperazinemethanamine with 4-(1H-imidazol-1-yl)benzenesulfonyl chloride to obtain the title compound.
Workup
- customIn a manner similar to Preparation 3
Sources & evidence
- ORD record
- ord-ed71e40d35634d618a760f72e5f6de8b
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05051422
Reaction notes
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