Tetrahydrofuran → 5-{[6-(Methylsulfonyl)pyridin-3-yl]oxy}-7-(tetrahydro-2H-pyran-4-yloxy)-1H-indole-2-carbothioamide
Reaction equation
[CH3:1][S:2](=[O:3])(=[O:4])[c:5]1[cH:6][cH:7][c:8]([O:11][c:12]2[cH:13][c:14]3[cH:15][c:16]([C:28](=[O:29])[NH2:30])[nH:17][c:18]3[c:19]([O:21][CH:22]3[CH2:23][CH2:24][O:25][CH2:26][CH2:27]3)[cH:20]2)[cH:9][n:10]1.[CH3:31][O:32][c:33]1[cH:34][cH:35][c:36]([P:37]2(=[S:40])[S:38][P:39]([c:41]3[cH:42][cH:43][c:44]([O:45][CH3:46])[cH:47][cH:48]3)(=[S:49])[S:50]2)[cH:51][cH:52]1.[O:53]1[CH2:54][CH2:55][CH2:56][CH2:57]1>>[CH3:1][S:2](=[O:3])(=[O:4])[c:5]1[cH:6][cH:7][c:8]([O:11][c:12]2[cH:13][c:14]3[cH:15][c:16]([C:28]([NH2:30])=[S:40])[nH:17][c:18]3[c:19]([O:21][CH:22]3[CH2:23][CH2:24][O:25][CH2:26][CH2:27]3)[cH:20]2)[cH:9][n:10]1Participants
4
Sources & evidence
- ORD record
- ord-b18d121d36c144a1ae9dc6a249d03e26
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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