Chloride → 6-(4-Tert.butyl-phenylsulphonylamino)-4-(2-hydroxy-ethoxy)-5-(3-methoxy-phenoxy)-pyrimidine-2-carboxylic acid phenylamide
Reaction equation
[C:24]([CH3:25])([CH3:26])([CH3:27])[c:28]1[cH:29][cH:30][c:31]([S:34](=[O:35])(=[O:36])[NH:37][c:38]2[c:39]([O:51][c:52]3[cH:53][c:54]([O:58][CH3:59])[cH:55][cH:56][cH:57]3)[c:40]([O:47][CH2:48][CH2:49][OH:50])[n:41][c:42]([C:44](=[O:45])[OH:46])[n:43]2)[cH:32][cH:33]1.[CH3:60][C:61]#[N:62].[Cl-:1].[NH2:17][c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1.[O:2]=[C:3]1[N:4]([P:5]([N:6]2[CH2:7][CH2:8][O:9][C:10]2=[O:11])(=[O:12])[OH:13])[CH2:14][CH2:15][O:16]1>>[NH:17]([c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1)[C:44]([c:42]1[n:41][c:40]([O:47][CH2:48][CH2:49][OH:50])[c:39]([O:51][c:52]2[cH:53][c:54]([O:58][CH3:59])[cH:55][cH:56][cH:57]2)[c:38]([NH:37][S:34]([c:31]2[cH:30][cH:29][c:28]([C:24]([CH3:25])([CH3:26])[CH3:27])[cH:33][cH:32]2)(=[O:35])=[O:36])[n:43]1)=[O:45]Participants
6
Reactant 5
Product 1
Sources & evidence
- ORD record
- ord-8c0e4bcf65094c42805127d80dcc2e30
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
Loading…