N,N-Dimethyl-1,3-propanediamine → N-(3-dimethylaminopropyl)-3-methoxy-4-nitro-benzamide
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][C:17]=1[N+:18]([O-:20])=[O:19])[C:6]([NH:8][C@@H:9]1[CH2:13][CH2:12][N:11]([CH3:14])[CH2:10]1)=[O:7].CN(C)CCCN>>[CH3:14][N:11]([CH3:10])[CH2:12][CH2:13][CH2:9][NH:8][C:6](=[O:7])[C:5]1[CH:15]=[CH:16][C:17]([N+:18]([O-:20])=[O:19])=[C:3]([O:2][CH3:1])[CH:4]=1Participants
3
Procedure
The title compound was prepared by an analogous method to the preparation of Intermediate 188, on a 9.28 mmol scale utilising N,N-dimethylpropane-1,3-diamine (Aldrich; 948 mg, 9.28 mmol), as a brown solid (2.33 g, 90%)
Sources & evidence
- ORD record
- ord-3a4e08784ae34b368270540d56a71ad2
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709471B2
Reaction notes
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