5-Aminoindole → 2-Methyl-6(thieno[3,2-b]pyridin-7-yloxy)-benzofuran-3-carboxylic acid (1H-indol-5-yl)-amide
Reaction equation
[CH3:1][c:2]1[o:3][c:4]2[c:5]([c:6]1[C:7](=[O:8])[Cl:9])[cH:10][cH:11][c:12]([O:14][c:15]1[c:16]3[c:17]([n:18][cH:19][cH:20]1)[cH:21][cH:22][s:23]3)[cH:13]2.[NH2:24][c:25]1[cH:26][c:27]2[cH:28][cH:29][nH:30][c:31]2[cH:32][cH:33]1>>[CH3:1][c:2]1[o:3][c:4]2[c:5]([c:6]1[C:7](=[O:8])[NH:24][c:25]1[cH:26][c:27]3[cH:28][cH:29][nH:30][c:31]3[cH:32][cH:33]1)[cH:10][cH:11][c:12]([O:14][c:15]1[c:16]3[c:17]([n:18][cH:19][cH:20]1)[cH:21][cH:22][s:23]3)[cH:13]2Participants
3
Sources & evidence
- ORD record
- ord-a93b692df5ae49b3981c2a74431be4e1
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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