Bromide ion → 4-Bromo-3-methyl-2-methylsulfonylaniline
Reaction equation
[Br-:19].[Br-:20].[Br-:21].[C:1](=[O:2])([O-:3])[O-:4].[CH2:22]([N+:23]([CH2:24][CH2:25][CH2:26][CH3:27])([CH2:28][CH2:29][CH2:30][CH3:31])[CH2:32][CH2:33][CH2:34][CH3:35])[CH2:36][CH2:37][CH3:38].[CH2:39]([N+:40]([CH2:41][CH2:42][CH2:43][CH3:44])([CH2:45][CH2:46][CH2:47][CH3:48])[CH2:49][CH2:50][CH2:51][CH3:52])[CH2:53][CH2:54][CH3:55].[CH2:56]([N+:57]([CH2:58][CH2:59][CH2:60][CH3:61])([CH2:62][CH2:63][CH2:64][CH3:65])[CH2:66][CH2:67][CH2:68][CH3:69])[CH2:70][CH2:71][CH3:72].[CH3:73][C:74]#[N:75].[CH3:7][c:8]1[c:9]([S:15](=[O:16])(=[O:17])[CH3:18])[c:10]([NH2:11])[cH:12][cH:13][cH:14]1.[K+:5].[K+:6]>>[CH3:7][c:8]1[c:9]([S:15](=[O:16])(=[O:17])[CH3:18])[c:10]([NH2:11])[cH:12][cH:13][c:14]1[Br:19]Participants
7
Sources & evidence
- ORD record
- ord-f406cbca85e74cc1a5b1d628adc6b91d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
Loading…