Cyclohexanol → HCID 86754213, compound
Reaction equation
[ClH:1].Cl.[NH:3]1[CH2:8][CH2:7][CH:6]([N:9]2[CH2:14][CH2:13][N:12]([C:15]([NH:17][CH:18]3[CH2:23][CH2:22][N:21]([CH2:24][C:25]([OH:27])=[O:26])[CH2:20][CH2:19]3)=[O:16])[CH2:11][CH2:10]2)[CH2:5][CH2:4]1.[CH:28]1(O)[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1>>[ClH:1].[ClH:1].[ClH:1].[NH:3]1[CH2:8][CH2:7][CH:6]([N:9]2[CH2:10][CH2:11][N:12]([C:15]([NH:17][CH:18]3[CH2:23][CH2:22][N:21]([CH2:24][C:25]([O:27][CH:28]4[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]4)=[O:26])[CH2:20][CH2:19]3)=[O:16])[CH2:13][CH2:14]2)[CH2:5][CH2:4]1Participants
3
Procedure
Prepared from 4-[[4-(4-piperidinyl)-piperazin-1-yl]carbonylamino]piperidinoacetic acid dihydrochloride and cyclohexanol.
Sources & evidence
- ORD record
- ord-581939d7586f429690efbf9ebbe577ba
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05922717
Reaction notes
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