Acetyl chloride → HCID 178460175, compound
Reaction equation
[CH2:46]1[O:47][CH2:48][CH2:49][CH2:50]1.[CH3:35][CH2:36][N:37]([CH2:38][CH3:39])[CH2:40][CH3:41].[CH3:42][C:43]([Cl:44])=[O:45].[NH2:1][CH2:2][CH2:3][N:4]1[C:5](=[O:34])[C:6]([CH3:32])([CH3:33])[c:7]2[cH:8][cH:9][c:10]([C:13](=[O:14])[N:15]([CH:16]3[CH2:17][N:18]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:19][CH2:20][CH2:21]3)[CH:29]([CH3:30])[CH3:31])[cH:11][c:12]21>>[NH:1]([CH2:2][CH2:3][N:4]1[C:5](=[O:34])[C:6]([CH3:32])([CH3:33])[c:7]2[cH:8][cH:9][c:10]([C:13](=[O:14])[N:15]([CH:16]3[CH2:17][N:18]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:19][CH2:20][CH2:21]3)[CH:29]([CH3:30])[CH3:31])[cH:11][c:12]21)[C:43]([CH2:40][CH3:41])=[O:45]Participants
5
Sources & evidence
- ORD record
- ord-2dd43f6ab694458e9c1cae0ab7f7170b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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