p-Toluenesulfonic acid → N-[1-(1H-1,2,3-benzotriazol-1-yl)-3,3-dimethylbutyl]-4-bromobenzamide
Reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[O:7])=[CH:4][CH:3]=1.[CH3:11][C:12]([CH3:17])([CH3:16])[CH2:13][CH:14]=O.[NH:18]1[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=2[N:20]=[N:19]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[N:18]1([CH:14]([NH:8][C:6](=[O:7])[C:5]2[CH:9]=[CH:10][C:2]([Br:1])=[CH:3][CH:4]=2)[CH2:13][C:12]([CH3:17])([CH3:16])[CH3:11])[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=2[N:20]=[N:19]1Participants
5
Procedure
A suspension of 4-bromobenzamide, 3,3-dimethylbutanal, benzotriazole, and p-toluenesulfonic acid was processed as described in Example 53A to provide the desired product.
Sources & evidence
- ORD record
- ord-e8de5c5206c4421ea84e33ad5027e5d4
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645968B2
Reaction notes
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