3-(5-bromo-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-one → ethyl [3-(3-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-2-oxo-2,3-dihydro-1H-indol-1-yl]acetate
Reaction equation
[Br:1][c:2]1[cH:3][cH:4][c:5]([OH:6])[c:7]([C:8]2([OH:9])[c:10]3[c:11]([cH:12][cH:13][cH:14][cH:15]3)[N:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[C:22]2=[O:23])[cH:24]1.[OH:25][C:26]1([c:42]2[cH:43][c:44]3[c:49]([cH:50][c:51]2[OH:52])[CH2:48][CH2:47][CH2:46][CH2:45]3)[C:27](=[O:41])[N:28]([CH2:35][C:36](=[O:37])[O:38][CH2:39][CH3:40])[c:29]2[cH:30][cH:31][cH:32][cH:33][c:34]21>>[CH:26]1([c:42]2[cH:43][c:44]3[c:49]([cH:50][c:51]2[OH:52])[CH2:48][CH2:47][CH2:46][CH2:45]3)[C:27](=[O:41])[N:28]([CH2:35][C:36](=[O:37])[O:38][CH2:39][CH3:40])[c:29]2[cH:30][cH:31][cH:32][cH:33][c:34]21Participants
3
Reactant 2
Product 1
Sources & evidence
- ORD record
- ord-152111e4ebeb4be8b6c3ed1fc0abc21e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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