Pyridine-3-sulfonyl chloride → N-{3-[5-(2-Chloro-4-pyrimidinyl)-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-3-pyridinesulfonamide
Reaction equation
[Cl:1][c:2]1[n:3][c:4](-[c:5]2[s:6][c:7]([CH:8]([CH3:9])[CH3:10])[n:11][c:12]2-[c:13]2[cH:14][c:15]([NH:16][S:17]([c:18]3[c:19]([F:20])[cH:21][cH:22][cH:23][c:24]3[F:25])(=[O:26])=[O:27])[cH:28][cH:29][cH:30]2)[cH:31][cH:32][n:33]1.[Cl:34][c:35]1[n:36][cH:37][cH:38][c:39](-[c:41]2[c:42](-[c:52]3[c:53]([F:59])[c:54]([NH2:55])[cH:56][cH:57][cH:58]3)[n:43][c:44]([N:46]3[CH2:47][CH2:48][O:49][CH2:50][CH2:51]3)[s:45]2)[n:40]1.[n:60]1[cH:61][c:62]([S:66](=[O:67])(=[O:68])[Cl:69])[cH:63][cH:64][cH:65]1>>[Cl:34][c:35]1[n:36][cH:37][cH:38][c:39](-[c:41]2[c:42](-[c:52]3[c:53]([F:59])[c:54]([NH:55][S:66]([c:62]4[cH:61][n:60][cH:65][cH:64][cH:63]4)(=[O:67])=[O:68])[cH:56][cH:57][cH:58]3)[n:43][c:44]([N:46]3[CH2:47][CH2:48][O:49][CH2:50][CH2:51]3)[s:45]2)[n:40]1Participants
4
Reactant 3
Product 1
Sources & evidence
- ORD record
- ord-0281c5accef9461aafb6cae0861cb1db
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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