2-Aminoquinoline → 3-Cyclohexyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-quinolin-2-yl-propionamide
Reaction equation
[CH:1]1([CH2:7][CH:8]([C:9](=[O:10])[OH:11])[N:12]2[C:13](=[O:21])[c:14]3[cH:15][cH:16][cH:17][cH:18][c:19]3[CH2:20]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1.[CH:33]1([CH2:34][CH:35]([N:36]2[CH2:37][c:38]3[c:39]([cH:40][cH:41][cH:42][cH:43]3)[C:44]2=[O:45])[C:46]([NH:47][c:48]2[s:49][cH:50][cH:51][n:52]2)=[O:53])[CH2:54][CH2:55][CH2:56][CH2:57][CH2:58]1.[NH2:22][c:23]1[n:24][c:25]2[cH:26][cH:27][cH:28][cH:29][c:30]2[cH:31][cH:32]1>>[CH:1]1([CH2:7][CH:8]([C:9](=[O:11])[NH:22][c:23]2[n:24][c:25]3[cH:26][cH:27][cH:28][cH:29][c:30]3[cH:31][cH:32]2)[N:12]2[C:13](=[O:21])[c:14]3[cH:15][cH:16][cH:17][cH:18][c:19]3[CH2:20]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
4
Sources & evidence
- ORD record
- ord-12bd5d1a9a3c43bba9b6ed6019388b98
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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