Chloride → 2-Thiazol-2-yl-pyrimidine-5-carboxylic acid (5-fluoro-3-methyl-indol-1-yl)-amide
Reaction equation
[CH3:38][O:39][c:40]1[n:41][c:42]([O:43][CH3:44])[n:45][c:46]([N+:47]2([CH3:48])[CH2:49][CH2:50][O:51][CH2:52][CH2:53]2)[n:54]1.[CH:28]([N:29]([CH:30]([CH3:31])[CH3:32])[CH2:33][CH3:34])([CH3:35])[CH3:36].[Cl-:15].[Cl-:37].[F:16][c:17]1[cH:18][c:19]2[c:20]([CH3:27])[cH:21][n:22]([NH3+:26])[c:23]2[cH:24][cH:25]1.[O:55]=[CH:56][N:57]([CH3:58])[CH3:59].[s:1]1[c:2](-[c:6]2[n:7][cH:8][c:9]([C:12](=[O:13])[OH:14])[cH:10][n:11]2)[n:3][cH:4][cH:5]1>>[s:1]1[c:2](-[c:6]2[n:7][cH:8][c:9]([C:12](=[O:14])[NH:26][n:22]3[cH:21][c:20]([CH3:27])[c:19]4[cH:18][c:17]([F:16])[cH:25][cH:24][c:23]43)[cH:10][n:11]2)[n:3][cH:4][cH:5]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-2364de815a2541138fe5df649acd69d2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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