2-Thiazolesulfonyl chloride → N-{3-[5-(2-Chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-1,3-thiazole-2-sulfonamide
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:49]3[c:50]([F:56])[c:51]([NH2:52])[cH:53][cH:54][cH:55]3)[n:43][c:44]([CH:46]([CH3:47])[CH3:48])[s:45]2)[n:40]1.[s:57]1[c:58]([S:62](=[O:63])(=[O:64])[Cl:65])[n:59][cH:60][cH:61]1>>[Cl:34][c:35]1[n:36][cH:37][cH:38][c:39](-[c:41]2[c:42](-[c:49]3[c:50]([F:56])[c:51]([NH:52][S:62]([c:58]4[s:57][cH:61][cH:60][n:59]4)(=[O:63])=[O:64])[cH:53][cH:54][cH:55]3)[n:43][c:44]([CH:46]([CH3:47])[CH3:48])[s:45]2)[n:40]1Participants
4
Reactant 3
Product 1
Sources & evidence
- ORD record
- ord-4bae647a25c1486ba92a8cd7f793a903
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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