4-Methoxybenzenesulfonyl chloride → HCID 69209442, compound
Reaction equation
[Cl:1][C:2]1[C:3]([Cl:18])=[C:4]2[NH:10][C:9]([C:11]3[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=3)=[N:8][C:5]2=[N:6][CH:7]=1.[CH3:19][O:20][C:21]1[CH:26]=[CH:25][C:24]([S:27](Cl)(=[O:29])=[O:28])=[CH:23][CH:22]=1>>[Cl:1][C:2]1[C:3]([Cl:18])=[C:4]2[NH:10][C:9]([C:11]3[CH:17]=[CH:16][C:14]([NH:15][S:27]([C:24]4[CH:23]=[CH:22][C:21]([O:20][CH3:19])=[CH:26][CH:25]=4)(=[O:29])=[O:28])=[CH:13][CH:12]=3)=[N:8][C:5]2=[N:6][CH:7]=1Participants
3
Procedure
By a procedure similar to Example 261 but using 4-(6,7-dichloro-1H-imidazo[4,5-b]pyridin-2-yl)aniline and 4-methoxybenzenesulfonyl chloride the title compound was obtained as the trifluoroacetate.
Sources & evidence
- ORD record
- ord-f9643f7886d244dd8d838622f75c909d
- Source dataset
- uspto-grants-2008_08
- Patent number
- US07410966B2
Reaction notes
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