3-Acetamidopyrrolidine → HCID 22053561, compound
Reaction equation
[C:40]([CH3:41])(=[O:42])[NH:43][CH:44]1[CH2:45][NH:46][CH2:47][CH2:48]1.[F:1][C:2]([c:3]1[cH:4][c:5]([CH2:6][N:7]2[C:8](=[O:30])[c:9]3[c:10]([n:15][c:16]([S:26]([CH3:27])(=[O:28])=[O:29])[n:17][c:18]3-[c:19]3[c:20]([CH3:25])[cH:21][cH:22][cH:23][cH:24]3)[NH:11][CH2:12][CH2:13][CH2:14]2)[cH:31][c:32]([C:34]([F:35])([F:36])[F:37])[cH:33]1)([F:38])[F:39]>>[F:1][C:2]([c:3]1[cH:4][c:5]([CH2:6][N:7]2[C:8](=[O:30])[c:9]3[c:10]([n:15][c:16]([N:46]4[CH2:45][CH:44]([NH:43][C:40]([CH3:41])=[O:42])[CH2:48][CH2:47]4)[n:17][c:18]3-[c:19]3[c:20]([CH3:25])[cH:21][cH:22][cH:23][cH:24]3)[NH:11][CH2:12][CH2:13][CH2:14]2)[cH:31][c:32]([C:34]([F:35])([F:36])[F:37])[cH:33]1)([F:38])[F:39]Participants
3
Sources & evidence
- ORD record
- ord-e0b6815074194c4b89332ac77c6b9508
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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