2-Aminothiazole → 6-bromo-1-isopropyl-1H-indole-3-carboxylic acid thiazol-2-ylamide
Reaction equation
[Br:20][N:21]1[C:22](=[O:23])[CH2:24][CH2:25][C:26]1=[O:27].[Br:28][c:29]1[cH:30][cH:31][c:32]2[c:33]([C:41](=[O:42])[OH:43])[cH:34][n:35]([CH:38]([CH3:39])[CH3:40])[c:36]2[cH:37]1.[CH2:50]([Cl:51])[Cl:52].[NH2:44][c:45]1[s:46][cH:47][cH:48][n:49]1.[c:1]1([P:2]([c:3]2[cH:4][cH:5][cH:6][cH:7][cH:8]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[cH:15][cH:16][cH:17][cH:18][cH:19]1>>[Br:28][c:29]1[cH:30][cH:31][c:32]2[c:33]([C:41](=[O:43])[NH:44][c:45]3[s:46][cH:47][cH:48][n:49]3)[cH:34][n:35]([CH:38]([CH3:39])[CH3:40])[c:36]2[cH:37]1Participants
6
Sources & evidence
- ORD record
- ord-b959aeb767e8448cb11cca32d6d9a015
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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