Anthranilic Acid → HCID 11502343, compound
Reaction equation
[C:1]([OH:10])(=O)[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[CH2:11]([NH2:14])[CH2:12][CH3:13].[CH:15](=O)[C:16]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=1.Cl[CH2:26][CH2:27][CH2:28]Br.[NH:30]1[CH2:35][CH2:34]C[CH2:32][CH2:31]1>>[CH2:11]([N:14]1[C:1](=[O:10])[C:2]2[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:4]=[C:15]1[C:16]1[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH2:32][CH2:31][N:30]2[CH2:35][CH2:34][CH2:28][CH2:27][CH2:26]2)=[CH:18][CH:17]=1)[CH2:12][CH3:13]Participants
6
Procedure
The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, propylamine, 4-anisaldehyde, 1-chloro-3-bromopropane and piperidine.
Workup
- customThe entitled compound was obtained
Sources & evidence
- ORD record
- ord-38bac8be85614c58bac41e70036d0775
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960394B2
Reaction notes
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