1-(2,4-Xylyl)piperazine → HCID 71261384, compound
Reaction equation
[O:1]=[C:2]1[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[C:8]1[CH:18]=[CH:17][C:11]([C:12]([O:14]CC)=O)=[CH:10][CH:9]=1.[CH3:19][C:20]1[CH:25]=[C:24]([CH3:26])[CH:23]=[CH:22][C:21]=1[N:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1>>[CH3:19][C:20]1[CH:25]=[C:24]([CH3:26])[CH:23]=[CH:22][C:21]=1[N:27]1[CH2:28][CH2:29][N:30]([C:12]([C:11]2[CH:10]=[CH:9][C:8]([N:3]3[CH2:4][CH2:5][CH2:6][CH2:7][C:2]3=[O:1])=[CH:18][CH:17]=2)=[O:14])[CH2:31][CH2:32]1Participants
3
Procedure
Using ethyl 4-(2-oxopiperidin-1-yl)benzoate (247 mg) and 1-(2,4-dimethylphenyl)piperazine (190 mg) and by the reaction and treatment in the same manner as in Example 109, the title compound (219 mg) was obtained.
Workup
- customby the reaction and treatment in the same manner as in Example 109
Sources & evidence
- ORD record
- ord-67ed98d1178243c2abca73e860776d75
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816079B2
Reaction notes
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