N-(3-Aminopropyl)morpholine → HCID 86720667, compound
Reaction equation
C([C:4]1[C:9]2[CH:10]=[CH:11][N:12]([C:13]([C:15]3[C:23]([Cl:24])=[CH:22][C:18]([C:19]([OH:21])=O)=[CH:17][C:16]=3[Cl:25])=[O:14])[C:8]=2[CH:7]=[CH:6][N:5]=1)(=O)C.[N:26]1([CH2:32][CH2:33][CH2:34][NH2:35])[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1>>[C:13]([NH:12][C:4]1[C:9]2[CH:10]=[CH:11][N:12]([C:13]([C:15]3[C:16]([Cl:25])=[CH:17][C:18]([C:19]([NH:35][CH2:34][CH2:33][CH2:32][N:26]4[CH2:31][CH2:30][O:29][CH2:28][CH2:27]4)=[O:21])=[CH:22][C:23]=3[Cl:24])=[O:14])[C:8]=2[CH:7]=[CH:6][N:5]=1)(=[O:14])[CH3:15]Participants
3
Procedure
This was prepared analogously from 4-[(4-acetyl-1H-pyrrolo[3,2-c]pyridin-1-yl)carbonyl]-3,5-dichlorobenzoic acid and 3-(morpholin-4-yl)propylamine.
Sources & evidence
- ORD record
- ord-40b8dffcfa864cf1ad4782372e8663a5
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09364466B2
Reaction notes
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