Furan-2-sulfonyl Chloride → N-{3-[5-(2-Chloro-4-pyrimidinyl)-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2-furansulfonamide
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.[o:60]1[c:61]([S:65](=[O:66])(=[O:67])[Cl:68])[cH:62][cH:63][cH:64]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:65]([c:61]4[o:60][cH:64][cH:63][cH:62]4)(=[O:66])=[O:67])[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-847e8c57a46e433f8feba90679251d11
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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