Sulfuryl chloride → N-[1-(4-Amino-thieno[3,2-c]pyridin-2-ylmethyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-4-(tetrahydropyran-4-yloxymethyl)-benzenesulfonamide
Reaction equation
[NH2:20][c:21]1[n:22][cH:23][cH:24][c:25]2[c:26]1[cH:27][c:28]([CH2:30][CH:31]([C:32](=[O:33])[N:34]1[CH2:35][CH2:36][CH:37]([CH3:40])[CH2:38][CH2:39]1)[NH:41][S:42](=[O:43])(=[O:44])[c:45]1[cH:46][cH:47][c:48]([O:49][CH:50]3[CH2:51][CH2:52][O:53][CH2:54][CH2:55]3)[cH:56][cH:57]1)[s:29]2.[O:6]1[CH2:7][CH2:8][CH:9]([O:12][CH2:13][c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[CH2:10][CH2:11]1.[S:1]([Cl:2])([Cl:3])(=[O:4])=[O:5]>>[O:6]1[CH2:7][CH2:8][CH:9]([O:12][CH2:13][c:14]2[cH:15][cH:16][c:17]([S:42]([NH:41][CH:31]([CH2:30][c:28]3[cH:27][c:26]4[c:21]([NH2:20])[n:22][cH:23][cH:24][c:25]4[s:29]3)[C:32](=[O:33])[N:34]3[CH2:35][CH2:36][CH:37]([CH3:40])[CH2:38][CH2:39]3)(=[O:43])=[O:44])[cH:18][cH:19]2)[CH2:10][CH2:11]1Participants
4
Reactant 3
Product 1
Sources & evidence
- ORD record
- ord-b4d8af274fb54a208394a32feeedd68c
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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