1-azetidin-3-ylpyrrolidine → HCID 178466324, compound
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][c:7]([O:44][CH2:45][CH3:46])[c:8]([C:11]2=[N:15][C:14]([CH3:16])([c:17]3[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]3)[C:13]([CH3:24])([c:25]3[cH:26][cH:27][c:28]([Cl:31])[cH:29][cH:30]3)[N:12]2[C:32](=[O:33])[N:34]2[CH2:35][CH2:36][CH:37]([CH2:40][C:41](=[O:42])[OH:43])[CH2:38][CH2:39]2)[cH:9][n:10]1.[NH:47]1[CH2:48][CH:49]([N:51]2[CH2:52][CH2:53][CH2:54][CH2:55]2)[CH2:50]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][c:7]([O:44][CH2:45][CH3:46])[c:8]([C:11]2=[N:15][C:14]([CH3:16])([c:17]3[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]3)[C:13]([CH3:24])([c:25]3[cH:26][cH:27][c:28]([Cl:31])[cH:29][cH:30]3)[N:12]2[C:32](=[O:33])[N:34]2[CH2:35][CH2:36][CH:37]([CH2:40][C:41](=[O:42])[N:47]3[CH2:48][CH:49]([N:51]4[CH2:52][CH2:53][CH2:54][CH2:55]4)[CH2:50]3)[CH2:38][CH2:39]2)[cH:9][n:10]1Participants
3
Sources & evidence
- ORD record
- ord-8e8f658856154113ba1030b7c57c57bc
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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