Reaction equation
F[C:2]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([NH2:18])(=[O:17])=[O:16])[CH:6]=[CH:5][C:3]=1[NH2:4].[CH3:19]C1C=C(Br)C=CC=1N.FC1C=C(Br)C=CC=1N>>[CH3:19][C:2]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([NH2:18])(=[O:17])=[O:16])[CH:6]=[CH:5][C:3]=1[NH2:4]Participants
4
Procedure
This compound was prepared by the method described for 2-fluoro-4-(2 -aminosulfonylphenyl)aniline described in EXAMPLE 8 by starting with 2-methyl-4-bromoaniline rather than 2-fluoro-4-bromoaniline.
Workup
- customThis compound was prepared by the method
Sources & evidence
- ORD record
- ord-529b3f8a63594da8b3924d5d73385209
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998424
Linked notes
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