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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401992Generated: October 26, 2026

Lithium Hexamethyldisilazide → 5-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1401992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 2773527—
ReactantN-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 57732216—
SolventTetrahydrofuranHCID 8028—
Product5-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 59436614—

Reaction Steps

To a solution of (N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine (Preparation 14, 40.6 g, 0.1619 mol) in anhydrous tetrahydrofuran (600. mL), cooled to −70° C., under nitrogen was added lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (1 M in tetrahydrofuran, 161.9 mL, 0.161.9 mol) drop wise. The reaction mixture was warmed to room temperature and stirred for 1 hour before cooling to −70° C. A solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (40 g, 0.1619 mol) in tetrahydrofuran (200.0 mL) was added dropwise. After complete addition, the reaction mixture was gradually warmed to room temperature and stirred for 1 hour. Reaction mixture was quenched with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. Organic layer was washed with water and saturated aqueous sodium chloride solution. Crude residue was purified by column chromatography eluting with ethyl acetate:hexane (gradient 1:19 to 3:17, by volume) to afford the title compound as a white solid, 46 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-41fde5b91b194b9e8b706160133d9704
Source noteuspto-grants-2014_12