Hydrochloric Acid → tert-butyl N-[2-(3-cyanoazetidin-1-yl)-1-cyclopropyl-2-oxoethyl]carbamate
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][CH:9]([C:10](=[O:11])[OH:12])[CH:13]1[CH2:14][CH2:15]1.[C:39](#[N:40])[CH:41]1[CH2:42][NH:43][CH2:44]1.[CH:45]([N:46]([CH2:47][CH3:48])[CH:49]([CH3:50])[CH3:51])([CH3:52])[CH3:53].[Cl:55][CH2:56][Cl:57].[ClH:38].[ClH:54].[F:16][B-:17]([F:18])([F:19])[F:20].[OH2:58].[n:21]1([O:22][C:23]([N:24]([CH3:25])[CH3:26])=[N+:27]([CH3:28])[CH3:29])[c:30]2[cH:31][cH:32][cH:33][cH:34][c:35]2[n:36][n:37]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][CH:9]([C:10](=[O:12])[N:43]1[CH2:42][CH:41]([C:39]#[N:40])[CH2:44]1)[CH:13]1[CH2:14][CH2:15]1Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-c3dab52cb0c34cdb93bae3111244bc28
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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