Anthranilic Acid → HCID 44563063, compound
Reaction equation
[C:1]([OH:10])(=O)[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH:18](=O)[C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=1.Cl[CH2:29][CH2:30][CH2:31]Br.[NH:33]1[CH2:38][CH2:37]C[CH2:35][CH2:34]1>>[N:33]1([CH2:38][CH2:37][CH2:26][O:25][C:22]2[CH:23]=[CH:24][C:19]([C:18]3[N:11]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)[C:1](=[O:10])[C:2]4[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=4)[N:4]=3)=[CH:20][CH:21]=2)[CH2:34][CH2:35][CH2:31][CH2:30][CH2:29]1Participants
6
Procedure
The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, aniline, 4-anisaldehyde, 1-chloro-3-bromopropane and piperidine.
Workup
- customThe entitled compound was obtained
Sources & evidence
- ORD record
- ord-f2321a9632e647758c8a1a0484d9052c
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960394B2
Reaction notes
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