Potassium Cation → N-(2-bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxymethyl-3-methyl-benzenesulfonamide

Reaction equation

[Br:5][c:6]1[n:7][cH:8][c:9]([Cl:24])[cH:10][c:11]1[NH:12][S:13](=[O:14])(=[O:15])[c:16]1[cH:17][c:18]([CH3:23])[c:19]([Cl:22])[cH:20][cH:21]1.[C:25](=[O:26])([O-:27])[O-:28].[CH2:31]1[O:32][CH2:33][CH2:34][CH2:35]1.[CH3:1][O:2][CH2:3][Cl:4].[K+:29].[K+:30]>>[CH3:1][O:2][CH2:3][N:12]([c:11]1[c:6]([Br:5])[n:7][cH:8][c:9]([Cl:24])[cH:10]1)[S:13](=[O:14])(=[O:15])[c:16]1[cH:17][c:18]([CH3:23])[c:19]([Cl:22])[cH:20][cH:21]1

Participants

Reactant 5

HCID 813Potassium Cation2×

HCID 7864Chloromethyl Methyl Ether

HCID 8028Tetrahydrofuran

HCID 19660Carbonate Ion

HCID 86606891N-(2-bromo-5-chloro-pyridin-3-yl)-4-chloro-3-methyl-benzenesulfonamide

Product 1

HCID 57942201N-(2-bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxymethyl-3-methyl-benzenesulfonamide

Sources & evidence

ORD record: ord-c48e6e7606ab455e97e80be9bdc5ee8a
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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