N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide → N-cyclopropyl-N-[1-(4-dimethylaminobenzyl)piperidin-4-yl]-3-trifluoromethylbenzenesulfonamide
Reaction equation
[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)(=[O:7])=[O:6])[CH2:3][CH2:2]1.Br[CH2:25][C:26]1[CH:31]=[CH:30][C:29]([N:32]([CH3:34])[CH3:33])=[CH:28][CH:27]=1>>[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][N:21]([CH2:25][C:26]3[CH:31]=[CH:30][C:29]([N:32]([CH3:34])[CH3:33])=[CH:28][CH:27]=3)[CH2:20][CH2:19]2)[S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:15])[F:16])[CH:9]=2)(=[O:6])=[O:7])[CH2:3][CH2:2]1Participants
3
Procedure
Similarly, N-cyclopropyl-N-[1-(4-dimethylaminobenzyl)piperidin-4-yl]-3-trifluoromethylbenzenesulfonamide was prepared from N-cyclopropyl-N-piperidin-4-yl-3-trifluoromethylbenzenesulfonamide and 1-bromomethyl-4-dimethylaminobenzene.
Sources & evidence
- ORD record
- ord-b0975497045b4c6da73428f869d63111
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000174B2
Reaction notes
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