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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46348생성일: 2026년 10월 23일

Lithium Hexamethyldisilazide → N-(2,4-Dimethoxybenzyl)-2,4,5-trifluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/46348

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2,4,5-Trifluorobenzenesulfonyl chlorideHCID 2776979—
반응물N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 57732216—
용매TetrahydrofuranHCID 8028—
생성물N-(2,4-Dimethoxybenzyl)-2,4,5-trifluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 5943658375%

반응 단계

To a solution of (N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine (Preparation 14, 13 g, 51.73 mmol) in dry tetrahydrofuran (150 ml) at −70° C. under argon atmosphere was added 1 M lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide in tetrahydrofuran (56.9 ml, 56.9 mmol) dropwise. The reaction mixture was allowed to warm up to room temperature and stirred for 1 h. It was again cooled to −70° C. and a tetrahydrofuran (50 ml) solution of 2,4,5-trifluorobenzenesulfonyl chloride (11.9 g, 51.73 mmol) was added dropwise to it at this temperature. After complete addition, reaction mixture was gradually allowed to warm up to room temperature and stirred for 1 hour. The reaction mixture was quenched with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride solution. Crude product was purified over 100-200 silica gel using 5-15% v/v ethyl acetate in hexane to give 17 g (75%) of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a3854f3601e3420b8231e1fdd086add6
출처 메모uspto-grants-2013_09