Hydrochloric Acid → tert-butyl N-[1-(3-cyanoazetidin-1-yl)-1-oxopropan-2-yl]carbamate
Reaction equation
[C:1](=[O:2])([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])[NH:8][CH:9]([CH3:10])[C:11](=[O:12])[OH:13].[C:37](#[N:38])[CH:39]1[CH2:40][NH:41][CH2:42]1.[CH3:55][CH2:56][O:57][C:58](=[O:59])[CH3:60].[CH:43]([N:44]([CH2:45][CH3:46])[CH:47]([CH3:48])[CH3:49])([CH3:50])[CH3:51].[Cl:52][CH2:53][Cl:54].[ClH:36].[F:14][B-:15]([F:16])([F:17])[F:18].[OH2:61].[n:19]1([O:20][C:21]([N:22]([CH3:23])[CH3:24])=[N+:25]([CH3:26])[CH3:27])[c:28]2[cH:29][cH:30][cH:31][cH:32][c:33]2[n:34][n:35]1>>[C:1](=[O:2])([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])[NH:8][CH:9]([CH3:10])[C:11](=[O:13])[N:41]1[CH2:40][CH:39]([C:37]#[N:38])[CH2:42]1Participants
10
Reactant 9
Product 1
Sources & evidence
- ORD record
- ord-5dc080d53e8b426a8a154cce7da28b7d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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