HCID 68926914, compound → HCID 25063729, compound
Reaction equation
[ClH:1].Cl.[CH:3]([N:16]1[C@@H:21](C)[CH2:20][N:19]([CH2:23][C:24]([OH:26])=[O:25])[C@H:18]([CH3:27])[CH2:17]1)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl.Cl.C(N1[C@H](C)CN(CC(O)=O)[C@@H](C)C1)(C1C=CC=CC=1)C1C=CC=CC=1>>[ClH:1].[ClH:1].[CH:3]([N:16]1[CH2:21][CH2:20][N:19]([CH2:23][C:24]([OH:26])=[O:25])[C@H:18]([CH3:27])[CH2:17]1)([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
a mixture of 2-((2R,5S)-4-benzhydryl-2,5-dimethylpiperazin-1-yl)acetic acid dihydrochloride and 2-((2S,5R)-4-benzhydryl-2,5-dimethylpiperazin-1-yl)acetic acid dihydrochloride MS (ESI, pos. ion) m/z: 339 (M+1).
Sources & evidence
- ORD record
- ord-877b362746a2454cb0b8d71a9cdef5c8
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08735383B2
Reaction notes
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