Hippuric Acid → HCID 59689125, compound
Reaction equation
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]([NH2:20])[C:10]2[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][CH:11]=2)=[CH:5][CH:4]=1.[C:23](O)(=[O:34])[CH2:24][NH:25][C:26]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:27]>>[F:1][C:2]([F:21])([F:22])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]([NH:20][C:23]([CH2:24][NH:25][C:26](=[O:27])[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[O:34])[C:10]2[CH:15]=[CH:14][C:13]([C:16]([F:17])([F:18])[F:19])=[CH:12][CH:11]=2)=[CH:5][CH:4]=1Participants
3
Procedure
Prepared in analogy to example 1.1 from C,C-bis-(4-trifluoromethyl-phenyl)-methylamine (example 4.1) and hippuric acid.
Sources & evidence
- ORD record
- ord-6d4cf72263eb4f4f86893b440a87c50c
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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