Hydrochloric Acid → HCID 18321468, compound
Reaction equation
[CH3:1][N:2]([CH3:27])[CH2:3][CH2:4][CH2:5][CH:6]([C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][N:17](CC3C=CC=CC=3)[CH2:16][CH2:15]2)=[CH:10][CH:9]=1)O.[ClH:28]>[Pd].C(OCC)(=O)C.CO>[ClH:28].[ClH:28].[CH3:27][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][CH2:6][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)=[CH:10][CH:9]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepared analogously to example A20b) from 4-[4-[4-(dimethylamino)-1-hydroxybutyl]phenyl]-1-(phenylmethyl)piperazine by catalytic hydrogenation in the presence of palladium/charcoal and hydrochloric acid in a quantitative yield. Colourless, amorphous substance of Rf=0.37 (eluant:ethyl acetate/methanol 50/50/0.5 v/v/v).
Sources & evidence
- ORD record
- ord-18dba26e8e8948fd939be7197b40dddb
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07498325B2
Reaction notes
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