1,1'-Carbonyldiimidazole → HCID 9827440, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][C:9]([OH:11])=O)[CH:2]=1.C1N=CN(C(N2C=NC=C2)=O)C=1.[S:24]1[C:28]2[S:29][CH2:30][C:31]3[CH:48]=[CH:47][CH:46]=[CH:45][C:32]=3[C:33](=[C:34]3[CH2:39][CH2:38][N:37]([CH2:40][CH2:41][CH2:42][CH2:43][NH2:44])[CH2:36][CH2:35]3)[C:27]=2[CH:26]=[CH:25]1>>[S:24]1[C:28]2[S:29][CH2:30][C:31]3[CH:48]=[CH:47][CH:46]=[CH:45][C:32]=3[C:33](=[C:34]3[CH2:39][CH2:38][N:37]([CH2:40][CH2:41][CH2:42][CH2:43][NH:44][C:9](=[O:11])[CH2:8][CH2:7][C:3]4[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=4)[CH2:36][CH2:35]3)[C:27]=2[CH:26]=[CH:25]1Participants
4
Procedure
Batch size: 1.4 g (9.0 mmol) 3-(3-pyridyl)-propionic acid, 1.6 g (9.9 mmol) CDI and 4.0 g (10.8 mmol) 4-[4-(4,9-dihydro-thieno[2,3-b]-benzo[e]-thiepin-4-yliden)-piperidin-1-yl]butylamine.
Sources & evidence
- ORD record
- ord-9985d78b721845388518d8fba2593b6f
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06593344B1
Reaction notes
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