Pyridine → HCID 20238652, compound
Reaction equation
[Cl:57][CH2:58][Cl:59].[F:38][C:39]([F:40])([F:41])[C:42]([O:43][C:44](=[O:45])[C:46]([F:47])([F:48])[F:49])=[O:50].[cH:51]1[cH:52][cH:53][n:54][cH:55][cH:56]1.[n:1]1[c:2]2[c:3]([n:4][o:5]1)[c:6]([CH:10]1[C:11]([C:33](=[O:34])[O:35][CH2:36][CH3:37])=[C:12]([CH:26]([O:27][CH2:28][CH3:29])[O:30][CH2:31][CH3:32])[NH:13][C:14]([C:21]([F:22])([F:23])[F:24])([OH:25])[CH:15]1[C:16](=[O:17])[O:18][CH2:19][CH3:20])[cH:7][cH:8][cH:9]2>>[n:1]1[c:2]2[c:3]([n:4][o:5]1)[c:6]([CH:10]1[C:11]([C:33](=[O:34])[O:35][CH2:36][CH3:37])=[C:12]([CH:26]([O:27][CH2:28][CH3:29])[O:30][CH2:31][CH3:32])[NH:13][C:14]([C:21]([F:22])([F:23])[F:24])=[C:15]1[C:16](=[O:17])[O:18][CH2:19][CH3:20])[cH:7][cH:8][cH:9]2Participants
5
Sources & evidence
- ORD record
- ord-d024c90fb11446f6a96fbc06e49e6b7d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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