Anthranilamide → HCID 2732583, compound
Reaction equation
[C:1]([NH2:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[CH:11]1([CH:17]=O)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1>>[CH:11]1([CH:17]2[NH:10][C:1](=[O:9])[C:2]3[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=3)[NH:4]2)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1Participants
3
Procedure
Anthranilamide was transformed by Method G (using cyclohexanecarboxaldehyde). M.p. 172–174° C.
Sources & evidence
- ORD record
- ord-8b4c62afbefe4e14b83ae8e146ca3383
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235548B2
Reaction notes
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