Hydrochloric Acid → Ethyl 2-[2-(7-chloro-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl]-6-methyl-3-oxo-6-heptenoate
Reaction equation
[CH3:3][C:4]([CH2:5][CH2:6][C:7]([CH2:8][C:9](=[O:10])[O:11][CH2:12][CH3:13])=[O:14])=[CH2:15].[CH3:40][N:41]([CH3:42])[CH:43]=[O:44].[Cl:16][CH:17]1[N:18]([c:27]2[n:28][c:29]3[n:30][c:31]([Cl:37])[cH:32][cH:33][c:34]3[cH:35][cH:36]2)[C:19](=[O:26])[c:20]2[cH:21][cH:22][cH:23][cH:24][c:25]21.[ClH:38].[H-:1].[Na+:2].[OH2:39]>>[CH3:3][C:4]([CH2:5][CH2:6][C:7]([CH:8]([C:9](=[O:10])[O:11][CH2:12][CH3:13])[CH:17]1[N:18]([c:27]2[n:28][c:29]3[n:30][c:31]([Cl:37])[cH:32][cH:33][c:34]3[cH:35][cH:36]2)[C:19](=[O:26])[c:20]2[cH:21][cH:22][cH:23][cH:24][c:25]21)=[O:14])=[CH2:15]Participants
8
Reactant 7
Product 1
Sources & evidence
- ORD record
- ord-7c129ff510064e728eddcff0efa4929b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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