Anthranilic Acid → HCID 11523989, 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]([NH2:13])[CH3:12].[CH:14](=O)[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([O:21][CH3:22])[CH:16]=1.Cl[CH2:25][CH2:26][CH2:27]Br.[NH:29]1[CH2:34][CH2:33]C[CH2:31][CH2:30]1>>[CH2:11]([N:13]1[C:1](=[O:10])[C:2]2[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:4]=[C:14]1[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([O:21][CH2:22][CH2:31][CH2:30][N:29]2[CH2:34][CH2:33][CH2:27][CH2:26][CH2:25]2)[CH:16]=1)[CH3:12]Participants
6
Procedure
The entitled compound was obtained according to the method of Example 1 but starting from anthranilic acid, ethylamine, 3-anisaldehyde, 1-chloro-3-bromopropane and piperidine.
Workup
- customThe entitled compound was obtained
Sources & evidence
- ORD record
- ord-216b3c03ccff475b9eedc8c1c11ba692
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960394B2
Reaction notes
Loading…