4-Chlorobenzoyl chloride → HCID 68806589, compound
Reaction equation
[CH:1]1([N:6]2[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][CH2:14][C:15]([NH:17][OH:18])=[NH:16])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:19][C:20]1[CH:28]=[CH:27][C:23]([C:24](Cl)=O)=[CH:22][CH:21]=1>>[ClH:19].[CH:1]1([N:6]2[CH2:7][CH2:8][CH:9]([CH2:12][CH2:13][CH2:14][C:15]3[N:16]=[C:24]([C:23]4[CH:27]=[CH:28][C:20]([Cl:19])=[CH:21][CH:22]=4)[O:18][N:17]=3)[CH2:10][CH2:11]2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
3
Procedure
The title compound was prepared by a similar procedure to that described in Example 3, starting from 4-(1-cyclopentylpiperidin-4-yl)-N-hydroxybutyramidine and 4-chlorobenzoyl chloride.
Sources & evidence
- ORD record
- ord-29fd1ad938a94c6aa000924743e5dbaa
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07332508B2
Reaction notes
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