1-(2,4-Xylyl)piperazine → HCID 58484634, compound
Reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][C:3]=1[F:11].[CH3:12][C:13]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][C:14]=1[N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1>>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:23]2[CH2:24][CH2:25][N:20]([C:14]3[CH:15]=[CH:16][C:17]([CH3:19])=[CH:18][C:13]=3[CH3:12])[CH2:21][CH2:22]2)=[O:8])=[CH:4][C:3]=1[F:11]Participants
3
Procedure
Using 4-bromo-3-fluorobenzoic acid (5 g) and 1-(2,4-dimethylphenyl)piperazine (4 g) and by the reaction and treatment in the same manner as in Preparation Example 109, the title compound (7 g) was obtained.
Workup
- customby the reaction and treatment in the same manner
- customas in Preparation Example 109
Sources & evidence
- ORD record
- ord-45e0d86c90b947adbe10e1fc2b5893f2
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816079B2
Reaction notes
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