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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401772생성일: 2026년 10월 25일

Sodium Hydroxide → 4-[(1,2,4-Thiadiazol-5-ylamino)sulfonyl]benzoic acid

https://huagongshe.com/reaction/401772

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물5-Amino-1,2,4-thiadiazoleHCID 290274—
반응물LithiumHCID 3028194—
반응물Methyl 4-[(pentafluorophenoxy)sulfonyl]benzoateHCID 57732203—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-[(1,2,4-Thiadiazol-5-ylamino)sulfonyl]benzoic acidHCID 5773221443%

반응 단계

To a solution of 5-amino-1,2,4-thiadiazole (58 mg, 0.574 mmol, 1.1 eq) in THF (5 ml) was added, 1,1,3,3,3-Hexanemethyldisilazane lithium salt (LiHMDS, 1M in THF, 1.15 ml, 1.2 mmol, 2.2 eq) and the reaction mixture stirred at 50° C. for 5 minutes. Methyl 4-[(pentafluorophenoxy)sulfonyl]benzoate (Preparation 28, 196 mg, 0.513 mmol, 1 eq) was added and the reaction monitored. On the disappearance of the starting materials the reaction mixture was quenched with water (5 ml), diluted with ethyl acetate (10 ml), washed with saturated sodium hydrogen carbonate, dried over sodium sulphate, filtered and evaporated in vacuo. The residue was dissolved in dioxane (5 ml) and a solution of sodium hydroxide (100 mg, 2.5 mmol, 4.3 eq) in water (2 ml) was added and the reaction mixture stirred at room temperature for 30 minutes. The reaction mixture was partitioned between ethyl acetate (5 ml) and water (5 ml), the aqueous phase was acidified with concentrated HCl, extracted into ethyl acetate (10 ml), dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was triturated with DCM to yield the title compound as a pale yellow solid (64 mg, 0.22 mmol, 43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741934B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-389e8b09b8204af3a58e19e7c1a0ce60
출처 메모uspto-grants-2014_06