4-Phenylbenzoyl chloride → HCID 59657778, compound
Reaction equation
[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([C:12]([NH:14][OH:15])=[NH:13])[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2].[C:16]1([C:22]2[CH:30]=[CH:29][C:25]([C:26](Cl)=O)=[CH:24][CH:23]=2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[C:22]1([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:23]=[CH:24][C:25]([C:26]2[O:15][N:14]=[C:12]([CH:9]3[CH2:10][CH2:11][N:6]([CH:3]([CH2:4][CH3:5])[CH2:1][CH3:2])[CH2:7][CH2:8]3)[N:13]=2)=[CH:29][CH:30]=1Participants
3
Procedure
The title compound was prepared by a similar procedure to that described in Example 35a, starting from 1-(1-ethylpropyl)-N-hydroxypiperidine-4-carboxamidine and 4-phenylbenzoyl chloride.
Sources & evidence
- ORD record
- ord-d312b6a12a574bd59d177c5bd7f2736a
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07332508B2
Reaction notes
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