1,4,7-Triazacyclononane → HCID 68858920, compound
Reaction equation
[NH:1]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Br[CH:11]1[N:15]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:14](=[O:24])[CH2:13][CH2:12]1>>[CH2:17]([O:16][N:15]1[CH:11]([N:1]2[CH2:9][CH2:8][N:7]([CH:11]3[N:15]([O:16][CH2:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:14](=[O:24])[CH2:13][CH2:12]3)[CH2:6][CH2:5][N:4]([CH:11]3[N:15]([O:16][CH2:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:14](=[O:24])[CH2:13][CH2:12]3)[CH2:3][CH2:2]2)[CH2:12][CH2:13][C:14]1=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
From 1,4,7-triazacyclononane (1.1.3), 5-bromo-1-benzyloxy-2-pyrrolidone (1.2.6.11) and base.
Sources & evidence
- ORD record
- ord-68800475f6954dd5b8b9a2b1a6d88da8
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06387891B2
Reaction notes
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