4-Chlorobenzhydrylamine hydrochloride → HCID 59689113, 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.[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][C:26]([NH:28][CH2:29][C:30](O)=[O:31])=[O:27])=[CH:20][CH:19]=1>>[Cl:17][C:18]1[CH:19]=[CH:20][C:21]([CH2:24][CH2:25][C:26]([NH:28][CH2:29][C:30](=[O:31])[NH:14][CH:7]([C:6]2[CH:5]=[CH:4][C:3]([Cl:2])=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:27])=[CH:22][CH:23]=1Participants
3
Procedure
Prepared in analogy to example 1.1 from rac-4-chlorobenzhydrylamine hydrochloride and [3-(4-chloro-phenyl)-propionylamino]-acetic acid (Example 2.1).
Sources & evidence
- ORD record
- ord-99ee94588b8a4a0bb8ac3c18035a4926
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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