2-Thiophenesulfonyl chloride → HCID 9831249, compound
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][cH:7][c:8]([S:11](=[O:12])(=[O:13])[NH:14][c:15]2[n:16][c:17]([CH:35]3[CH2:36][CH2:37]3)[n:18][c:19]([O:30][CH2:31][CH2:32][CH2:33][NH2:34])[c:20]2[O:21][c:22]2[c:23]([O:28][CH3:29])[cH:24][cH:25][cH:26][cH:27]2)[cH:9][cH:10]1.[s:38]1[c:39]([S:43](=[O:44])(=[O:45])[Cl:46])[cH:40][cH:41][cH:42]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[cH:6][cH:7][c:8]([S:11](=[O:12])(=[O:13])[NH:14][c:15]2[n:16][c:17]([CH:35]3[CH2:36][CH2:37]3)[n:18][c:19]([O:30][CH2:31][CH2:32][CH2:33][NH:34][S:43]([c:39]3[s:38][cH:42][cH:41][cH:40]3)(=[O:44])=[O:45])[c:20]2[O:21][c:22]2[c:23]([O:28][CH3:29])[cH:24][cH:25][cH:26][cH:27]2)[cH:9][cH:10]1Participants
3
Sources & evidence
- ORD record
- ord-1e6b12b5313c4ddb95bed1741d4a1ecb
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction notes
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