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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 509101생성일: 2026년 10월 27일

Lithium Hexamethyldisilazide → 3-cyano-N-(2,4-dimethoxybenzyl)-4-fluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/509101

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물3-Cyano-4-fluorobenzenesulfonyl chlorideHCID 2778908—
반응물N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 57732216—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-cyano-N-(2,4-dimethoxybenzyl)-4-fluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 5804225471%

반응 조건

온도-78 °C

반응 단계

N-(2,4-Dimethoxybenzyl)-1,2,4-thiadiazol-5-amine (Preparation 18, 42.8 g, 170 mmol) was dissolved in anhydrous THF (600 mL) and stirred under a nitrogen atmosphere at −78° C. A 1M solution of LiHMDS in THF (238 mL, 238 mmol) was added dropwise over 30 minutes maintaining the temperature between −65° C. and −70° C. The reaction mixture was left at −78° C. for 5 minutes, then allowed to warm to −10° C. over 1.5 hours. Upon reaching −10° C., the brown reaction mixture was cooled to −78° C. again, and a solution of 3-cyano-4-fluorobenzene sulfonyl chloride (48.6 g, 221 mmol) in THF (200 mL) was added dropwise over 30 minutes maintaining the temperature between −65° C. and −70° C. The brown solution was allowed to warm gradually to ambient temperature and stirred overnight. The reaction mixture was diluted with ethyl acetate, washed with a saturated ammonium chloride solution, and extracting with further ethyl acetate. The combined organics were dried over MgSO4, filtered and concentrated in vacuo to afford a brown residue. The residue was purified by silica gel column chromatography (10%-30% ethyl acetate in heptane gradient elution) to afford the title compound as a white solid (52.3 g, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096558B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-3668af3c47694a34a552556dad9e70d9
출처 메모uspto-grants-2015_08