Benzoyl chloride, 3,4-dichloro- → HCID 68806471, 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:21]=[C:22]([CH:26]=[CH:27][C:28]=1[Cl:29])[C:23](Cl)=O>>[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:23]([C:22]4[CH:26]=[CH:27][C:28]([Cl:29])=[C:20]([Cl:19])[CH:21]=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 3,4-dichlorobenzoyl chloride.
Sources & evidence
- ORD record
- ord-1d9a7ef57a13457f8d3e7ced2b9ff30d
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799924B2
Reaction notes
Loading…