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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22765생성일: 2026년 10월 25일

4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chloride → 4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/22765

반응식

참여 물질

역할이름HCID투입량
반응물4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chlorideHCID 2776917—
반응물Benzenamine, 3-[2-(dimethylamino)ethoxy]-4-(trifluoromethyl)-HCID 17756283—
용매ChloroformHCID 6212—
생성물4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamideHCID 10165761—

반응 단계

To a mixture of 3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenylamine (0.10 g, 0.4 mmol) in CHCl3 (2.5 mL) was added 4-(3-chloro-2-cyano-phenoxy) benzenesulfonyl chloride (0.13 g, 0.4 mmol) at rt. After stirring at rt for 72 h, the solvent was evaporated and the residue was purified by vacuum filtration through silica gel eluting successively with 4% MeOH in CH2Cl2 and 10% MeOH in CH2Cl2 followed by a mixture of CH2Cl2, MeOH and conc. NH4OH (90:10:1). The solvent was removed from the desired fractions and the residue was recrystallized from a mixture of MeOH and EtOAc to afford the title compound as a white solid; yield 0.01 g (5%): LCMS 540 (M++H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849635B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f654829ee46b47468eb0b6f8ed977fb2
출처 메모uspto-grants-2005_02