1-[(3,4,5-Trimethoxyphenyl)methyl]piperazine → HCID 54468974, compound
Reaction equation
[C:1]1([C:7]2[CH:8]=[C:9]([CH:15]=[CH:16][CH:17]=2)[CH:10]=[CH:11][C:12]([OH:14])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:30]=[C:31]([O:35][CH3:36])[C:32]=1[O:33][CH3:34])[CH2:23][N:24]1[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1>>[C:1]1([C:7]2[CH:8]=[C:9]([CH:15]=[CH:16][CH:17]=2)[CH:10]=[CH:11][C:12]([N:27]2[CH2:26][CH2:25][N:24]([CH2:23][C:22]3[CH:30]=[C:31]([O:35][CH3:36])[C:32]([O:33][CH3:34])=[C:20]([O:19][CH3:18])[CH:21]=3)[CH2:29][CH2:28]2)=[O:14])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
Following a procedure similar to that described in Example 61, but using 0.500 g of 3-phenylcinnamic acid and 0.653 g of 1-(3,4,5-trimethoxybenzyl)piperazine, 0.897 g of the title compound was obtained as a powder.
Sources & evidence
- ORD record
- ord-05500ed8b5d04323b453e94a9281a672
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05369106
Reaction notes
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