Hydrochloric Acid → HCID 67595036, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][N:15]([CH:17]2[CH2:22][CH2:21][N:20]([C:23]3[CH:28]=[CH:27][C:26]([O:29][CH2:30][C:31]([O:33][CH3:34])=[O:32])=[CH:25][CH:24]=3)[CH2:19][CH2:18]2)[CH3:16])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:35]>>[ClH:35].[ClH:35].[CH3:34][O:33][C:31]([CH2:30][O:29][C:26]1[CH:27]=[CH:28][C:23]([N:20]2[CH2:21][CH2:22][CH:17]([N:15]([CH2:14][CH:11]3[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]3)[CH3:16])[CH2:18][CH2:19]2)=[CH:24][CH:25]=1)=[O:32]Participants
3
Procedure
Prepared from 4-[(1-tert-butyloxycarbonylpiperidin-4-yl)-N-methylmethylamino]-1-(4-methoxycarbonylmethyloxyphenyl)piperidine and ethereal hydrochloric acid.
Sources & evidence
- ORD record
- ord-ce89d77a81374a91b52e721311a14153
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05994356
Reaction notes
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