1-Phenylpiperazine → (4-Phenylpiperazin-1-yl)-(4-{[propyl-(4,5,6,7-tetrahydrobenzothiazol-6-yl)amino]methyl}phenyl)methanone
Reaction equation
[CH2:1]([N:4]([CH2:14][C:15]1[CH:23]=[CH:22][C:18]([C:19](Cl)=[O:20])=[CH:17][CH:16]=1)[CH:5]1[CH2:13][CH2:12][C:8]2[N:9]=[CH:10][S:11][C:7]=2[CH2:6]1)[CH2:2][CH3:3].[C:24]1([N:30]2[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.OCCCCNC(=O)C1C=CC=CC=1>>[C:24]1([N:30]2[CH2:35][CH2:34][N:33]([C:19]([C:18]3[CH:22]=[CH:23][C:15]([CH2:14][N:4]([CH2:1][CH2:2][CH3:3])[CH:5]4[CH2:13][CH2:12][C:8]5[N:9]=[CH:10][S:11][C:7]=5[CH2:6]4)=[CH:16][CH:17]=3)=[O:20])[CH2:32][CH2:31]2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1Participants
4
Reactant 3
Product 1
Procedure
Compound 43 is prepared from 42C and 1-phenyl-piperazine as described for 1D.
Sources & evidence
- ORD record
- ord-52258de052894e6fb976e27e386b6891
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08389555B2
Reaction notes
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