Reaction equation
[CH2:1]([C:3]1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23]([NH:25][S:26]([C:29]3[CH:34]=[CH:33][C:32](C)=[CH:31][CH:30]=3)(=[O:28])=[O:27])=[O:24])=[CH:16][CH:15]=2)[C:6]2=[N:7][C:8]([CH3:12])=[CH:9][C:10]([CH3:11])=[C:5]2[N:4]=1)[CH3:2].[Cl:36]C1C=CC=CC=1S(N=C=O)(=O)=O>>[Cl:36][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=1[S:26]([NH:25][C:23]([NH:22][CH2:21][CH2:20][C:17]1[CH:18]=[CH:19][C:14]([N:13]2[C:6]3=[N:7][C:8]([CH3:12])=[CH:9][C:10]([CH3:11])=[C:5]3[N:4]=[C:3]2[CH2:1][CH3:2])=[CH:15][CH:16]=1)=[O:24])(=[O:28])=[O:27]Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared according to the procedure described in step 10 of Example 1 from 2-[4-(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)phenyl]ethylamine (step 9 of Example 1) and 2-chlorobenzenesulfonyl isocyanate.
Sources & evidence
- ORD record
- ord-0dc85a9bc7e0469d97c1b8f3f440a831
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06710054B2
Linked notes
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