Hydrochloric Acid → 1-O-[(1-amino-2-propylsulfonylethylidene)amino] 4-O-tert-butyl 2-(3-cyclohexylpropyl)butanedioate
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][CH:8]([C:9](=[O:10])[OH:11])[CH2:12][CH2:13][CH2:14][CH:15]1[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]1)=[O:21].[CH3:23][N:24]([CH3:25])[CH2:26][CH2:27][CH2:28][N:29]=[C:30]=[N:31][CH2:32][CH3:33].[CH3:34][N:35]1[CH2:36][CH2:37][O:38][CH2:39][CH2:40]1.[Cl:63][CH2:64][Cl:65].[ClH:22].[OH2:41].[OH2:66].[OH:42][n:43]1[c:44]2[cH:45][cH:46][cH:47][cH:48][c:49]2[n:50][n:51]1.[OH:52][N:53]=[C:54]([CH2:55][S:56](=[O:57])(=[O:58])[CH2:59][CH2:60][CH3:61])[NH2:62]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][CH:8]([C:9]([O:10][N:53]=[C:54]([CH2:55][S:56](=[O:57])(=[O:58])[CH2:59][CH2:60][CH3:61])[NH2:62])=[O:11])[CH2:12][CH2:13][CH2:14][CH:15]1[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]1)=[O:21]Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-bcb7e5495a724813a9b5a01dc112f810
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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