Hydrochloric Acid → tert-butyl N-[1-[[3-(1H-indol-3-yl)-1-oxo-1-(4-oxospiro[3H-chromene-2,4'-piperidine]-1'-yl)propan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]carbamate
Reaction equation
[CH3:1][C:2]([CH3:3])([O:4][C:5](=[O:6])[NH:7][C:8]([C:9](=[O:10])[NH:11][CH:12]([C:13](=[O:14])[OH:15])[CH2:16][c:17]1[cH:18][nH:19][c:20]2[cH:21][cH:22][cH:23][cH:24][c:25]12)([CH3:26])[CH3:27])[CH3:28].[ClH:45].[NH:29]1[CH2:30][CH2:31][C:32]2([O:33][c:34]3[c:35]([cH:39][cH:40][cH:41][cH:42]3)[C:36](=[O:38])[CH2:37]2)[CH2:43][CH2:44]1>>[CH3:1][C:2]([CH3:3])([O:4][C:5](=[O:6])[NH:7][C:8]([C:9](=[O:10])[NH:11][CH:12]([C:13](=[O:14])[N:29]1[CH2:30][CH2:31][C:32]2([O:33][c:34]3[c:35]([cH:39][cH:40][cH:41][cH:42]3)[C:36](=[O:38])[CH2:37]2)[CH2:43][CH2:44]1)[CH2:16][c:17]1[cH:18][nH:19][c:20]2[cH:21][cH:22][cH:23][cH:24][c:25]12)([CH3:26])[CH3:27])[CH3:28]Participants
4
Sources & evidence
- ORD record
- ord-3a2a732b2163400297bde6941fc1ac5c
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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