Benzyl piperazine-1-carboxylate → HCID 14326640, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][CH:19]=[CH:18][C:4]=1[CH2:5][N:6]1[CH2:11][C:10](=[O:12])[N:9]([CH2:13][CH2:14][CH2:15]Cl)[C:8](=[O:17])[CH2:7]1.[CH2:22]([O:29][C:30]([N:32]1[CH2:37][CH2:36][NH:35][CH2:34][CH2:33]1)=[O:31])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[CH2:22]([O:29][C:30]([N:32]1[CH2:37][CH2:36][N:35]([CH2:15][CH2:14][CH2:13][N:9]2[C:10](=[O:12])[CH2:11][N:6]([CH2:5][C:4]3[CH:18]=[CH:19][CH:20]=[CH:21][C:3]=3[O:2][CH3:1])[CH2:7][C:8]2=[O:17])[CH2:34][CH2:33]1)=[O:31])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
Procedure
This compound was prepared according to the process described in Example 5 by condensing 4-(2-methoxybenzyl)-1-(3-chloropropyl)piperazine-2,6-dione with 4-benzyloxycarbonylpiperazine.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-f089ba9e565a48d8ad92ddd6bcdded02
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04877788
Reaction notes
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