4-Chlorobenzhydrylamine hydrochloride → HCID 59689137, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:16]=[CH:15][C:6]([CH:7]([NH2:14])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:5][CH:4]=1.[CH3:17][O:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][C:27]([NH:29][CH2:30][C:31](O)=[O:32])=[O:28])=[CH:21][CH:20]=1>>[Cl:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]([NH:14][C:31]([CH2:30][NH:29][C:27](=[O:28])[CH2:26][CH2:25][C:22]2[CH:21]=[CH:20][C:19]([O:18][CH3:17])=[CH:24][CH:23]=2)=[O:32])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:15][CH:16]=1Participants
3
Procedure
Prepared in analogy to example 1.1 from rac-4-chlorobenzhydrylamine hydrochloride and [3-(4-methoxy-phenyl)-propionylamino]-acetic acid (Example 2.2).
Sources & evidence
- ORD record
- ord-32ba8d0f75bf4be5944664bb0f19fc9c
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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