(2S,3S)-3-[(5-Methoxy-1-(trifluoromethyl)indan-6-yl)methylamino]-2-phenylpiperidine → (2S,3S)-3-[(5-Methoxy-1-(trifluoromethyl)indan-6-yl)methylamino]-2-phenylpiperidine dihydrochloride
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[CH2:12][NH:13][C@H:14]1[CH2:19][CH2:18][CH2:17][NH:16][C@H:15]1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH:8]([C:26]([F:29])([F:28])[F:27])[CH2:7][CH2:6]2.[ClH:30].Cl.FC(C1C=CC(OC(F)(F)F)=C(C=1)CN[C@H]1CCCN[C@H]1C1C=CC=CC=1)(F)C>>[ClH:30].[ClH:30].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[CH2:12][NH:13][C@H:14]1[CH2:19][CH2:18][CH2:17][NH:16][C@H:15]1[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[CH:8]([C:26]([F:29])([F:27])[F:28])[CH2:7][CH2:6]2Participants
3
Reactant 2
Product 1
Procedure
This compound was prepared from Compound 67 in the same manner of Compound 28.
Sources & evidence
- ORD record
- ord-e3a57d78e15941f290302e6309a85505
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506775B1
Reaction notes
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