Hydrochloric Acid → HCID 19602675, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][CH2:15][CH:16]2[CH2:21][CH2:20][N:19]([C:22]3[CH:27]=[CH:26][C:25]([O:28][CH2:29][C:30]([O:32][CH3:33])=[O:31])=[CH:24][CH:23]=3)[CH2:18][CH2:17]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:34]>>[ClH:34].[ClH:34].[CH3:33][O:32][C:30]([CH2:29][O:28][C:25]1[CH:26]=[CH:27][C:22]([N:19]2[CH2:20][CH2:21][CH:16]([CH2:15][NH:14][CH:11]3[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]3)[CH2:17][CH2:18]2)=[CH:23][CH:24]=1)=[O:31]Participants
3
Procedure
Prepared from 4-[(1-tert-butyloxycarbonylpiperidin-4-yl)aminomethyl]-1-(4-methoxycarbonylmethyloxyphenyl)piperidine and ethereal hydrochloric acid.
Sources & evidence
- ORD record
- ord-12a74435c5f14f8ea79ba8bc8b62473a
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05994356
Reaction notes
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