Dimethyl Sulfoxide → HCID 18184223, compound

HRID 2132607Notes

Reaction equation

HRID 2132607 reaction equation
[C:20]([CH3:21])([CH3:22])([CH3:23])[c:24]1[cH:25][cH:26][c:27]([S:30](=[O:31])(=[O:32])[NH2:33])[cH:28][cH:29]1.[CH3:34][S:35]([CH3:36])=[O:37].[Cl:1][c:2]1[n:3][c:4]([CH3:18])[n:5][c:6]([Cl:17])[c:7]1[O:8][c:9]1[c:10]([O:15][CH3:16])[cH:11][cH:12][cH:13][cH:14]1.[K:19].[OH2:38]>>[c:2]1([NH:33][S:30]([c:27]2[cH:26][cH:25][c:24]([C:20]([CH3:21])([CH3:22])[CH3:23])[cH:29][cH:28]2)(=[O:31])=[O:32])[n:3][c:4]([CH3:18])[n:5][c:6]([Cl:17])[c:7]1[O:8][c:9]1[c:10]([O:15][CH3:16])[cH:11][cH:12][cH:13][cH:14]1

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 962WaterHCID 2228724-tert-ButylbenzenesulfonamideHCID 5462222PotassiumHCID 219795994,6-Dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidine

Product 1

HCID 18184223HCID 18184223, compound

Sources & evidence

ORD record
ord-9d9f18986ec2463a91a6a27b2e9b4d5f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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