4-Cyclohexylbenzoyl chloride → HCID 68807187, compound
Reaction equation
[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][CH2:14][C:15]([NH:17][OH:18])=[NH:16])[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2].[CH:19]1([C:25]2[CH:33]=[CH:32][C:28]([C:29]([Cl:31])=O)=[CH:27][CH:26]=2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>>[ClH:31].[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][CH2:14][C:15]2[N:16]=[C:29]([C:28]3[CH:32]=[CH:33][C:25]([CH:19]4[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]4)=[CH:26][CH:27]=3)[O:18][N:17]=2)[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2]Participants
3
Procedure
The title compound was prepared by a similar procedure to that described in Example 3, starting from 4-(1-(1-ethylpropyl)piperidin-4-yl)-N-hydroxybutyramidine and 4-cyclohexyl benzoyl chloride.
Sources & evidence
- ORD record
- ord-f7d70a764ac0471ba9f89408770ee2d3
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799924B2
Reaction notes
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