Water → 4-(2-Fluoro-4-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Reaction equation
[CH3:35][CH2:36][N:37]([CH2:38][CH3:39])[CH2:40][CH3:41].[CH3:55][C:56]#[N:57].[Cl:42][c:43]1[cH:44][c:45]([F:53])[c:46]([S:49](=[O:50])(=[O:51])[Cl:52])[cH:47][cH:48]1.[OH2:54].[OH:1][c:2]1[c:3]2[c:7]([c:8](-[c:11]3[n:12]([C:27](=[O:28])[O:29][C:30]([CH3:31])([CH3:32])[CH3:33])[c:13]4[cH:14][cH:15][c:16]([CH2:20][N:21]5[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]5)[cH:17][c:18]4[cH:19]3)[cH:9][cH:10]1)[C:6](=[O:34])[NH:5][CH2:4]2>>[O:1]([c:2]1[c:3]2[c:7]([c:8](-[c:11]3[n:12]([C:27](=[O:28])[O:29][C:30]([CH3:31])([CH3:32])[CH3:33])[c:13]4[cH:14][cH:15][c:16]([CH2:20][N:21]5[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]5)[cH:17][c:18]4[cH:19]3)[cH:9][cH:10]1)[C:6](=[O:34])[NH:5][CH2:4]2)[S:49]([c:46]1[c:45]([F:53])[cH:44][c:43]([Cl:42])[cH:48][cH:47]1)(=[O:50])=[O:51]Participants
6
Reactant 5
Product 1
Sources & evidence
- ORD record
- ord-565c8830359b44e6b7b325f4fa512f1b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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