4-Chloro-2-nitrobenzoic acid → HCID 59689135, compound
Reaction equation
Cl.[NH2:2][CH2:3][C:4]([NH:6][CH:7]([C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:5].[Cl:21][C:22]1[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[C:24]([N+:31]([O-:33])=[O:32])[CH:23]=1>>[Cl:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([NH:2][CH2:3][C:4](=[O:5])[NH:6][CH:7]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:27])=[C:24]([N+:31]([O-:33])=[O:32])[CH:23]=1Participants
3
Procedure
Prepared in analogy to example 1.12 from rac-2-amino-N-[(4-chloro-phenyl)-phenyl-methyl]-acetamide hydrochloride (Example 3.1) and 4-chloro-2-nitrobenzoic acid.
Sources & evidence
- ORD record
- ord-d906a48f891d4df480ac8ba19d416d2f
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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