Hydrochloric Acid → benzyl N-[4-amino-1-[[4-[2-(tert-butylcarbamoyl)-4-chloropyrrolidin-1-yl]-3-hydroxy-4-oxo-1-phenylbutan-2-yl]amino]-1,4-dioxobutan-2-yl]carbamate
Reaction equation
[C:2]([CH3:3])([CH3:4])([CH3:5])[NH:6][C:7]([CH:8]1[NH:9][CH2:10][CH:11]([Cl:13])[CH2:12]1)=[O:14].[CH2:15]([c:16]1[cH:17][cH:18][cH:19][cH:20][cH:21]1)[O:22][C:23](=[O:24])[NH:25][CH:26]([CH2:27][C:28]([NH2:29])=[O:30])[C:31](=[O:32])[NH:33][CH:34]([CH:35]([C:36](=[O:37])[OH:38])[OH:39])[CH2:40][c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1.[CH3:57][CH2:58][N:59]([CH2:60][CH3:61])[CH2:62][CH3:63].[CH3:64][N:65]([CH3:66])[CH:67]=[O:68].[ClH:1].[P:47]([C:48]#[N:49])([O:50][CH2:51][CH3:52])([O:53][CH2:54][CH3:55])=[O:56]>>[C:2]([CH3:3])([CH3:4])([CH3:5])[NH:6][C:7]([CH:8]1[N:9]([C:36]([CH:35]([CH:34]([NH:33][C:31]([CH:26]([NH:25][C:23]([O:22][CH2:15][c:16]2[cH:17][cH:18][cH:19][cH:20][cH:21]2)=[O:24])[CH2:27][C:28]([NH2:29])=[O:30])=[O:32])[CH2:40][c:41]2[cH:42][cH:43][cH:44][cH:45][cH:46]2)[OH:39])=[O:37])[CH2:10][CH:11]([Cl:13])[CH2:12]1)=[O:14]Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-eee264440262489bae53667d69b5ef38
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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