4-Bromoaniline → HCID 178503189, compound
Reaction equation
[CH3:1][S:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[CH:5][CH:4]=1.[Br:11][C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][CH:13]=1>>[Br:11][C:12]1[CH:18]=[CH:17][C:15]([NH:16][C:7]([C:6]2[CH:9]=[CH:10][C:3]([S:2][CH3:1])=[CH:4][CH:5]=2)=[NH:8])=[CH:14][CH:13]=1Participants
3
Procedure
The title compound was prepared from 4-methylthiobenzonitrile (17.3 g, 116 mmol) and 4-bromoaniline (20 g, 116 mmol) by following the procedure described in preparation 10 (29 g, yield 77.7%, purity 99.8% by HPLC). MS m/z:321.1/323.2 (M+).
Workup
- customdescribed in preparation 10 (29 g, yield 77.7%, purity 99.8% by HPLC)
Sources & evidence
- ORD record
- ord-4d6163f1474b45c28e432584801d2eb7
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365069B2
Reaction notes
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