Oxalyl chloride → HCID 86651138, compound
Reaction equation
[CH:1]1([C:4](=[O:5])[N:6]([CH2:7][CH3:8])[CH2:9][c:10]2[c:11](-[c:20]3[cH:21][c:22]([CH:30]([C:31](=[O:32])[OH:33])[CH3:34])[cH:23][c:24]([C:26]([F:27])([F:28])[F:29])[cH:25]3)[cH:12][cH:13][c:14]([C:16]([F:17])([F:18])[F:19])[cH:15]2)[CH2:2][CH2:3]1.[Cl:35][C:36]([C:37]([Cl:38])=[O:39])=[O:40]>>[CH:1]1([C:4](=[O:5])[N:6]([CH2:7][CH3:8])[CH2:9][c:10]2[c:11](-[c:20]3[cH:21][c:22]([CH:30]([C:31](=[O:32])[Cl:35])[CH3:34])[cH:23][c:24]([C:26]([F:27])([F:28])[F:29])[cH:25]3)[cH:12][cH:13][c:14]([C:16]([F:17])([F:18])[F:19])[cH:15]2)[CH2:2][CH2:3]1Participants
3
Sources & evidence
- ORD record
- ord-6840ec1c6bdf4d40b4f03f222aee473e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
Loading…