Hydrochloric Acid → 5-[4-(4-(2-(2-t-Butoxycarbonylaminopropanamido)-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione
Reaction equation
[C:30]([CH3:31])([CH3:32])([CH3:33])[O:34][C:35](=[O:36])[NH:37][CH:38]([C:39](=[O:40])[OH:41])[CH3:42].[CH3:64][CH2:65][O:66][C:67](=[O:68])[CH3:69].[CH:43]1([N:44]=[C:45]=[N:46][CH:47]2[CH2:48][CH2:49][CH2:50][CH2:51][CH2:52]2)[CH2:53][CH2:54][CH2:55][CH2:56][CH2:57]1.[ClH:1].[NH2:2][CH:3]([CH2:4][c:5]1[cH:6][cH:7][c:8]([O:9][c:10]2[cH:11][cH:12][c:13]([CH:14]=[C:15]3[C:16](=[O:21])[NH:17][C:18](=[O:20])[S:19]3)[cH:22][cH:23]2)[cH:24][cH:25]1)[C:26](=[O:27])[O:28][CH3:29].[O:59]=[CH:60][N:61]([CH3:62])[CH3:63].[OH2:58]>>[NH:2]([CH:3]([CH2:4][c:5]1[cH:6][cH:7][c:8]([O:9][c:10]2[cH:11][cH:12][c:13]([CH:14]=[C:15]3[C:16](=[O:21])[NH:17][C:18](=[O:20])[S:19]3)[cH:22][cH:23]2)[cH:24][cH:25]1)[C:26](=[O:27])[O:28][CH3:29])[C:39]([CH:38]([NH:37][C:35]([O:34][C:30]([CH3:31])([CH3:32])[CH3:33])=[O:36])[CH3:42])=[O:40]Participants
8
Reactant 7
Product 1
Sources & evidence
- ORD record
- ord-6df51a7336824cfb89fcdd1c24e4eaa2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction notes
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