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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 2,4,5-Trifluorobenzenesulfonyl chloride | HCID 2776979 | — |
| 반응물 | N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine | HCID 57732216 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(2,4-Dimethoxybenzyl)-2,4,5-trifluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 59436583 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541588B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-a3854f3601e3420b8231e1fdd086add6 |
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| 출처 메모 | uspto-grants-2013_09 |
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