Nicotinoyl chloride → HCID 59134180, compound
Reaction equation
[C:1]([c:2]1[cH:3][n:4][cH:5][cH:6][cH:7]1)(=[O:8])[Cl:9].[NH2:10][CH:11]1[CH2:12][N:13]([S:34](=[O:35])(=[O:36])[c:37]2[c:38]([Cl:44])[cH:39][c:40]([Cl:43])[cH:41][cH:42]2)[CH:14]2[N:15]([C:16]1=[O:17])[CH:18]([CH2:26][c:27]1[cH:28][cH:29][c:30]([Cl:33])[cH:31][cH:32]1)[C:19](=[O:25])[N:20]([CH:22]([CH3:23])[CH3:24])[CH2:21]2>>[C:1]([c:2]1[cH:3][n:4][cH:5][cH:6][cH:7]1)(=[O:8])[NH:10][CH:11]1[CH2:12][N:13]([S:34](=[O:35])(=[O:36])[c:37]2[c:38]([Cl:44])[cH:39][c:40]([Cl:43])[cH:41][cH:42]2)[CH:14]2[N:15]([C:16]1=[O:17])[CH:18]([CH2:26][c:27]1[cH:28][cH:29][c:30]([Cl:33])[cH:31][cH:32]1)[C:19](=[O:25])[N:20]([CH:22]([CH3:23])[CH3:24])[CH2:21]2Participants
3
Sources & evidence
- ORD record
- ord-09e1ce2440ac4f0088a24af38409ae0c
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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