1,4-Dioxane → HCID 178438869, compound
Reaction equation
[C:36](=[O:37])([c:38]1[nH:39][cH:40][cH:41][n:42]1)[c:43]1[nH:44][cH:45][cH:46][n:47]1.[CH2:1]([CH:2]=[CH2:3])[C:4]1([CH3:35])[C:5](=[O:34])[N:6]([CH:24]([CH2:25][NH:26][CH2:27][C:28]([CH3:29])([CH3:30])[OH:31])[CH2:32][CH3:33])[CH:7]([c:17]2[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]2)[CH:8]([c:10]2[cH:11][c:12]([Cl:16])[cH:13][cH:14][cH:15]2)[CH2:9]1.[O:48]1[CH2:49][CH2:50][O:51][CH2:52][CH2:53]1>>[CH2:1]([CH:2]=[CH2:3])[C:4]1([CH3:35])[C:5](=[O:34])[N:6]([CH:24]([CH2:25][N:26]2[CH2:27][C:28]([CH3:29])([CH3:30])[O:31][C:36]2=[O:37])[CH2:32][CH3:33])[CH:7]([c:17]2[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]2)[CH:8]([c:10]2[cH:11][c:12]([Cl:16])[cH:13][cH:14][cH:15]2)[CH2:9]1Participants
4
Sources & evidence
- ORD record
- ord-1fe2ffed23334a46bcb82ba70cf50755
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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