Chloride → 1-Cyano-1-isopropyl-2-benzoyl-1,2-dihydroisoquinoline
Reaction equation
[C:1](#[N:2])[CH:3]1[N:4]([C:13]([c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)=[O:20])[CH:5]=[CH:6][c:7]2[cH:8][cH:9][cH:10][cH:11][c:12]21.[CH2:28]([N+:29]([CH2:30][CH3:31])([CH2:32][CH3:33])[CH2:34][CH3:35])[c:36]1[cH:37][cH:38][cH:39][cH:40][cH:41]1.[CH:23]([CH3:24])([CH3:25])[Br:26].[Cl-:27].[Na+:22].[OH-:21]>>[C:1](#[N:2])[C:3]1([CH:23]([CH3:24])[CH3:25])[N:4]([C:13]([c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)=[O:20])[CH:5]=[CH:6][c:7]2[cH:8][cH:9][cH:10][cH:11][c:12]21Participants
7
Sources & evidence
- ORD record
- ord-4ca03943ca7847c3bd57efb99eec9bf2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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