1,4,7-Triazacyclononane → HCID 86583980, 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]C1>>[CH3:11][N:15]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:14]([CH2:13][N:1]1[CH2:9][CH2:8][N:7]([CH2:13][C:14](=[O:24])[N:15]([O:16][CH2:17][C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH3:11])[CH2:6][CH2:5][N:4]([CH2:13][C:14](=[O:24])[N:15]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH3:11])[CH2:3][CH2:2]1)=[O:24]Participants
3
Procedure
From 1,4,7-triazacyclononane (1.1.3), 5-bromo-1-benzyloxy-2-pyrrolidone (1.2.6.11) and base. 1.3.5.15 N,N′,N″-Tris(1-oxy-2-pyrrolidone-5-yl)-1,4,7-triazacyclononane.
Sources & evidence
- ORD record
- ord-2f00fb99b9814413b201b65927fc60a8
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06881732B2
Reaction notes
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