Oxalyl chloride → HCID 57166640, compound
Reaction equation
[CH:18]([c:19]1[cH:20][cH:21][cH:22][cH:23][cH:24]1)([c:25]1[cH:26][cH:27][cH:28][cH:29][cH:30]1)[N:31]([CH2:32][CH2:33][N:34]([CH2:35][CH2:36][CH2:37][CH2:38][NH2:39])[CH3:40])[CH3:41].[Cl:12][C:13]([C:14]([Cl:15])=[O:16])=[O:17].[n:1]1[cH:2][c:3]([CH:7]=[CH:8][C:9](=[O:10])[OH:11])[cH:4][cH:5][cH:6]1>>[n:1]1[cH:2][c:3]([CH:7]=[CH:8][C:9](=[O:11])[NH:39][CH2:38][CH2:37][CH2:36][CH2:35][N:34]([CH2:33][CH2:32][N:31]([CH:18]([c:19]2[cH:20][cH:21][cH:22][cH:23][cH:24]2)[c:25]2[cH:26][cH:27][cH:28][cH:29][cH:30]2)[CH3:41])[CH3:40])[cH:4][cH:5][cH:6]1Participants
4
Sources & evidence
- ORD record
- ord-055ea177dba642e985cb86eaa0c8d9ef
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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