Tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate → HCID 25204447, compound
Reaction equation
[CH3:1][S:2](=[O:3])(=[O:4])[c:5]1[cH:6][cH:7][c:8](-[n:11]2[c:12](=[O:31])[cH:13][c:14]([S:17][CH:18]3[CH2:19][CH2:20][N:21]([C:24](=[O:25])[O:26][C:27]([CH3:28])([CH3:29])[CH3:30])[CH2:22][CH2:23]3)[cH:15][cH:16]2)[cH:9][cH:10]1.[CH3:32][S:33]([c:34]1[cH:35][cH:36][c:37](-[n:38]2[cH:39][cH:40][c:41]([O:42][CH:43]3[CH2:44][CH2:45][N:46]([C:47]([O:48][C:49]([CH3:50])([CH3:51])[CH3:52])=[O:53])[CH2:54][CH2:55]3)[cH:56][c:57]2=[O:58])[cH:59][cH:60]1)(=[O:61])=[O:62]>>[CH3:1][S:2](=[O:3])(=[O:4])[c:5]1[cH:6][cH:7][c:8](-[n:11]2[c:12](=[O:31])[cH:13][c:14]([S:17][CH:18]3[CH2:19][CH2:20][N:21]([C:24](=[O:25])[O:26][CH:27]([CH3:28])[CH3:29])[CH2:22][CH2:23]3)[cH:15][cH:16]2)[cH:9][cH:10]1Participants
3
Sources & evidence
- ORD record
- ord-c93c818eef8d4132bdcc1970cd9e5bc7
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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