Hydrochloric Acid → HCID 19602702, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][N:16]2[CH2:21][CH2:20][N:19]([C:22]3[CH:27]=[CH:26][C:25]([O:28][CH:29]([C:38]([O:40][CH3:41])=[O:39])[CH2:30][C:31]4[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=4)=[CH:24][CH:23]=3)[CH2:18][CH2:17]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:42]>>[ClH:37].[ClH:42].[Cl:37][C:34]1[CH:35]=[CH:36][C:31]([CH2:30][CH:29]([C:38]([O:40][CH3:41])=[O:39])[O:28][C:25]2[CH:24]=[CH:23][C:22]([N:19]3[CH2:18][CH2:17][N:16]([CH2:15][CH2:14][CH:11]4[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]4)[CH2:21][CH2:20]3)=[CH:27][CH:26]=2)=[CH:32][CH:33]=1Participants
3
Procedure
Prepared from 4-[2-(1-tert-butyloxycarbonylpiperidin-4-yl)ethyl]-1-[4-(2-(4-chlorophenyl)-1-methoxycarbonylethyloxy)phenyl]piperazine and ethereal hydrochloric acid.
Sources & evidence
- ORD record
- ord-c200aaee36514e69a35f68b46923641b
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05994356
Reaction notes
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