Dimethyl Sulfoxide → HCID 51353708, compound

HRID 158331Notes

Reaction equation

HRID 158331 reaction equation
[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([S:9](=[O:10])(=[O:11])[NH:12][CH3:13])[cH:7][cH:8]1.[CH3:36][S:37]([CH3:38])=[O:39].[Cl:16][c:17]1[n:18][cH:19][cH:20][c:21](-[c:23]2[cH:24][c:25]3[c:26]([n:27][c:28]([NH:30][C:31]([CH3:32])=[O:33])[s:29]3)[cH:34][cH:35]2)[n:22]1.[H-:15].[Na+:14]>>[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([S:9](=[O:10])(=[O:11])[N:12]([CH3:13])[c:17]2[n:18][cH:19][cH:20][c:21](-[c:23]3[cH:24][c:25]4[c:26]([n:27][c:28]([NH:30][C:31]([CH3:32])=[O:33])[s:29]4)[cH:34][cH:35]3)[n:22]2)[cH:7][cH:8]1

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 923Sodium ionHCID 166653HydrideHCID 24974294-methoxy-N-methylbenzenesulfonamideHCID 51357685N-(6-(2-Chloropyrimidin-4-yl)benzo[d]thiazol-2-yl)acetamide

Product 1

HCID 51353708HCID 51353708, compound

Sources & evidence

ORD record
ord-0e4d439bba664e67aed45953ddc5dac1
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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