4-Butylbenzoyl chloride → HCID 68806767, compound
Reaction equation
[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]([NH:12][OH:13])=[NH:11])[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[CH2:14]([C:18]1[CH:26]=[CH:25][C:21]([C:22]([Cl:24])=O)=[CH:20][CH:19]=1)[CH2:15][CH2:16][CH3:17]>>[ClH:24].[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[N:11]=[C:22]([C:21]3[CH:25]=[CH:26][C:18]([CH2:14][CH2:15][CH2:16][CH3:17])=[CH:19][CH:20]=3)[O:13][N:12]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared by a similar procedure to that described in Example 56, starting from 1-isopropyl-N-hydroxypiperidine-4-carboxamidine and 4-butylbenzoyl chloride.
Sources & evidence
- ORD record
- ord-cf42df5a6e904a07ad9192042aa47e5c
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07332508B2
Reaction notes
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