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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808191Generated: October 25, 2026

Lithium → 3-Fluoro-4-[(1,2,4-thiadiazol-5-ylamino)sulfonyl]benzoic acid

https://huagongshe.com/reaction/1808191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithiumHCID 3028194—
Reactant4-(Chlorosulfonyl)-3-fluorobenzoic acidHCID 11310971—
ReactantN-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 57732216—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product3-Fluoro-4-[(1,2,4-thiadiazol-5-ylamino)sulfonyl]benzoic acidHCID 5773206416%

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine (Preparation 26, 500 mg, 2.1 mmol, 1.0 eq) was dissolved in THF (10 ml) and cooled to −78° C. 1,1,1,3,3,3-Hexanemethyldisilazane lithium salt (LiHMDS, 1M in THF, 4.2 ml, 4.19 mmol, 2.0 eq) was added dropwise and the reaction mixture stirred for a further 10 minutes. A solution of 4-(chlorosulfonyl)-3-fluorobenzoic acid (Preparation 9, 500 mg, 2.1 mmol, 1 eq) in THF (3 ml) was added dropwise and the reaction mixture stirred at −78° C. for 1 hour then at room temperature for 18 hours. The reaction mixture was diluted with brine, extracted into ethyl acetate, dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was passed through a SCX cartridge to remove remaining amine. The material was redissolved in 4M HCl in dioxane and stirred at room temperature for 2 hours. The resulting precipitate was collected by filtration and washed with diethylether to yield the title compound (100 mg, 0.33 mmol, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-5d150023172042c38609c17a69f9decb
Source noteuspto-grants-2013_01