Anthranilic Acid → HCID 11516386, compound
Reaction equation
[C:1]([OH:10])(=O)[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[CH3:11][NH2:12].[CH:13](=O)[C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1.Cl[CH2:24][CH2:25][CH2:26]Br.[NH:28]1[CH2:33][CH2:32]C[CH2:30][CH2:29]1>>[CH3:11][N:12]1[C:1](=[O:10])[C:2]2[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:4]=[C:13]1[C:14]1[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH2:30][CH2:29][N:28]2[CH2:33][CH2:32][CH2:26][CH2:25][CH2:24]2)=[CH:16][CH:15]=1Participants
6
Procedure
The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, methylamine, 4-anisaldehyde, 1-chloro-3-bromopropane and piperidine.
Workup
- customThe entitled compound was obtained
Sources & evidence
- ORD record
- ord-d21926430c7f419eb15f5372ccdaa379
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960394B2
Reaction notes
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