Reaction equation
[NH2:1][C:2]([NH:4][C:5]1[CH:9]=[C:8](Br)[S:7][C:6]=1[C:11]([NH2:13])=[O:12])=[O:3].[S:14]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[CH:16]=[C:15]1B(O)O>>[NH2:1][C:2]([NH:4][C:5]1[CH:9]=[C:8]([C:15]2[S:14][C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=3[CH:16]=2)[S:7][C:6]=1[C:11]([NH2:13])=[O:12])=[O:3]Participants
3
Procedure
The title compound was prepared from 3-[(aminocarbonyl)amino-5-bromothiophene-2-carboxamide and 1-benzothien-2-ylboronic acid in a similar manner to Example 11 (g).
Sources & evidence
- ORD record
- ord-adc4df26b1f04203ac53fb02abc42a4f
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07098240B2
Linked notes
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