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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401770생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/401770

반응식

참여 물질

역할이름HCID투입량
반응물LithiumHCID 3028194—
반응물4-(Chlorosulfonyl)-3-fluorobenzoic acidHCID 11310971—
반응물N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 57732216—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물3-Fluoro-4-[(1,2,4-thiadiazol-5-ylamino)sulfonyl]benzoic acidHCID 5773206416%

반응 조건

온도-78 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741934B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-b02317c19ec341018c4af3458b9a817a
출처 메모uspto-grants-2014_06