4-Chlorobenzoic Acid → HCID 59689107, compound
Reaction equation
[NH2:1][CH2:2][C:3]([NH:5][CH:6]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][CH:8]=1)=[O:4].[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25](O)=[O:26])=[CH:23][CH:22]=1>>[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([NH:1][CH2:2][C:3](=[O:4])[NH:5][CH:6]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][CH:8]=2)=[O:26])=[CH:23][CH:22]=1Participants
3
Procedure
Prepared in analogy to example 1.12 from rac-2-amino-N-(phenyl-p-tolyl-methyl)-acetamide (Example 3.3) and 4-chlorobenzoic acid.
Sources & evidence
- ORD record
- ord-a4e6c2b7f4a84022bbad74b3131c152b
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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