N-methyl-2-pyrrolidone → HCID 59624862, compound
Reaction equation
[CH3:45][N:46]1[CH2:47][CH2:48][CH2:49][C:50]1=[O:51].[CH:37]1([NH2:44])[CH2:38][CH2:39][CH:40]([NH2:43])[CH2:41][CH2:42]1.[Cl:1][c:2]1[cH:3][c:4]([N:21]([c:22]2[n:23][cH:24][cH:25][cH:26][cH:27]2)[CH2:28][c:29]2[cH:30][cH:31][c:32]([O:35][CH3:36])[cH:33][cH:34]2)[c:5]2[n:6]([n:7]1)[c:8]([C:11](=[O:12])[NH:13][c:14]1[cH:15][c:16]([F:20])[n:17][cH:18][cH:19]1)[cH:9][n:10]2>>[c:2]1([NH:44][CH:37]2[CH2:38][CH2:39][CH:40]([NH2:43])[CH2:41][CH2:42]2)[cH:3][c:4]([N:21]([c:22]2[n:23][cH:24][cH:25][cH:26][cH:27]2)[CH2:28][c:29]2[cH:30][cH:31][c:32]([O:35][CH3:36])[cH:33][cH:34]2)[c:5]2[n:6]([n:7]1)[c:8]([C:11](=[O:12])[NH:13][c:14]1[cH:15][c:16]([F:20])[n:17][cH:18][cH:19]1)[cH:9][n:10]2Participants
4
Sources & evidence
- ORD record
- ord-3e255608752348e494f83c3a5f964208
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
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