2-Thiophenesulfonyl chloride → HCID 18184247, compound
Reaction equation
[CH:1]([CH3:2])([CH3:3])[c:4]1[cH:5][cH:6][c:7]([S:10](=[O:11])(=[O:12])[NH:13][c:14]2[n:15][c:16](-[c:33]3[n:34][cH:35][cH:36][cH:37][n:38]3)[n:17][c:18]([O:29][CH2:30][CH2:31][NH2:32])[c:19]2[O:20][c:21]2[c:22]([O:27][CH3:28])[cH:23][cH:24][cH:25][cH:26]2)[n:8][cH:9]1.[s:39]1[c:40]([S:44](=[O:45])(=[O:46])[Cl:47])[cH:41][cH:42][cH:43]1>>[CH:1]([CH3:2])([CH3:3])[c:4]1[cH:5][cH:6][c:7]([S:10](=[O:11])(=[O:12])[NH:13][c:14]2[n:15][c:16](-[c:33]3[n:34][cH:35][cH:36][cH:37][n:38]3)[n:17][c:18]([O:29][CH2:30][CH2:31][NH:32][S:44]([c:40]3[s:39][cH:43][cH:42][cH:41]3)(=[O:45])=[O:46])[c:19]2[O:20][c:21]2[c:22]([O:27][CH3:28])[cH:23][cH:24][cH:25][cH:26]2)[n:8][cH:9]1Participants
3
Sources & evidence
- ORD record
- ord-e82903fe830e493eabbf01b45929f5d8
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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