Hydrochloric Acid → tert-Butyl 4-({[5-[(3,3-dimethylbutanoyl)amino]-1-(2-fluorobenzyl)-1H-indol-2-yl]-carbonyl}amino)phenylcarbamate
Reaction equation
[CH3:1][C:2]([CH2:3][C:4](=[O:5])[NH:6][c:7]1[cH:8][c:9]2[cH:10][c:11]([C:24](=[O:25])[OH:26])[n:12]([CH2:16][c:17]3[c:18]([F:23])[cH:19][cH:20][cH:21][cH:22]3)[c:13]2[cH:14][cH:15]1)([CH3:27])[CH3:28].[CH3:29][N:30]([CH3:31])[CH2:32][CH2:33][CH2:34][N:35]=[C:36]=[N:37][CH2:38][CH3:39].[CH3:56][N:57]([CH3:58])[c:59]1[cH:60][cH:61][n:62][cH:63][cH:64]1.[ClH:40].[NH2:41][c:42]1[cH:43][cH:44][c:45]([NH:48][C:49]([O:50][C:51]([CH3:52])([CH3:53])[CH3:54])=[O:55])[cH:46][cH:47]1.[O:65]=[CH:66][N:67]([CH3:68])[CH3:69]>>[CH3:1][C:2]([CH2:3][C:4](=[O:5])[NH:6][c:7]1[cH:8][c:9]2[cH:10][c:11]([C:24](=[O:26])[NH:41][c:42]3[cH:43][cH:44][c:45]([NH:48][C:49]([O:50][C:51]([CH3:52])([CH3:53])[CH3:54])=[O:55])[cH:46][cH:47]3)[n:12]([CH2:16][c:17]3[c:18]([F:23])[cH:19][cH:20][cH:21][cH:22]3)[c:13]2[cH:14][cH:15]1)([CH3:27])[CH3:28]Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-3bb0babc6e234810a258ad65e4ef4a0b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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