Anthranilic Acid → HCID 11641036, 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]([NH2:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH:19](=O)[C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=1.Cl[CH2:30][CH2:31][CH2:32]Br.[NH:34]1[CH2:39][CH2:38]C[CH2:36][CH2:35]1>>[CH2:11]([N:18]1[C:1](=[O:10])[C:2]2[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:4]=[C:19]1[C:20]1[CH:25]=[CH:24][C:23]([O:26][CH2:27][CH2:36][CH2:35][N:34]2[CH2:39][CH2:38][CH2:32][CH2:31][CH2:30]2)=[CH:22][CH:21]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
6
Procedure
The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, benzylamine, 4-anisaldehyde, 1-chloro-3-bromopropane and piperidine.
Workup
- customThe entitled compound was obtained
Sources & evidence
- ORD record
- ord-16319994c8764cf39d0a99d3a7d80684
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960394B2
Reaction notes
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