4-Bromoaniline → HCID 67040182, compound
Reaction equation
[CH:1]([C:4]1[CH:5]=[CH:6][C:7]2[C:12]([NH:13][C:14]3[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=3[S:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)[C:17](Cl)=[O:18])=[N:11][CH:10]=[N:9][C:8]=2[N:32]=1)([CH3:3])[CH3:2].[Br:33][C:34]1[CH:40]=[CH:39][C:37]([NH2:38])=[CH:36][CH:35]=1.NC1C=C(O)C(C)=CC=1>>[Br:33][C:34]1[CH:40]=[CH:39][C:37]([NH:38][C:17](=[O:18])[C:16]2[CH:20]=[CH:21][C:22]([S:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)=[C:14]([NH:13][C:12]3[C:7]4[CH:6]=[CH:5][C:4]([CH:1]([CH3:3])[CH3:2])=[N:32][C:8]=4[N:9]=[CH:10][N:11]=3)[CH:15]=2)=[CH:36][CH:35]=1Participants
4
Procedure
The product from Example 137B was reacted with 4-bromoaniline according to the procedure from Example 137C substituting 4-bromoaniline for 5-amino-o-cresol to provide the title compound as an off white solid after silica gel chromatography (109 mg, 85%).
Sources & evidence
- ORD record
- ord-92ed0544abd44ba3ae788ac974b33735
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910595B2
Reaction notes
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