Hydrochloric Acid → HCID 19602915, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][N:16]2[C:21](=[O:22])[CH2:20][N:19]([C:23]3[CH:28]=[CH:27][C:26]([O:29][CH2:30][C:31]([O:33][CH2:34][CH3:35])=[O:32])=[CH:25][CH:24]=3)[C:18](=[O:36])[CH2:17]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:37]>>[ClH:37].[CH2:34]([O:33][C:31]([CH2:30][O:29][C:26]1[CH:27]=[CH:28][C:23]([N:19]2[CH2:20][C:21](=[O:22])[N:16]([CH2:15][CH2:14][CH:11]3[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]3)[CH2:17][C:18]2=[O:36])=[CH:24][CH:25]=1)=[O:32])[CH3:35]Participants
3
Procedure
Prepared from 4-[2-(1-tert-butyloxycarbonylpiperidin-4-yl)ethyl]-1-(4-ethoxycarbonylmethyloxyphenyl)piperazin-2,5-dione and ethereal hydrochloric acid.
Sources & evidence
- ORD record
- ord-7f16b6389e4c4966b6905fd6f265e79c
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05994356
Reaction notes
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