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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379371생성일: 2026년 10월 26일

3,5-Bis(trifluoromethyl)benzyl bromide → Imnopitant

https://huagongshe.com/reaction/379371

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamideHCID 15481065—
용매TetrahydrofuranHCID 8028—
생성물ImnopitantHCID 980851875%

반응 단계

To a solution of 750 mg (2.32 mmol) N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide in 16 ml tetrahydrofuran, 3 ml of a 1 M solution (3 mmol) of potassium hexamethyldisilazide in tetrahydrofuran was added at room temperature. After 1 h, 0.43 ml (2.3 mmol) 3,5-bis(trifluoromethyl)benzyl bromide was added dropwise to the resulting suspension. The reaction was quenched with water after 1 h and the mixture was extracted with three 20 ml portions of ethyl acetate. The combined organic extracts were washed with saturated aqueous sodium chloride solution, dried with sodium sulfate and concentrated. Column chromatography gave 950 mg (74%) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide. The white foam was dissolved in a small amount of diethyl ether and treated with 2 ml 3 N hydrochloric acid solution in diethyl ether. Concentration afforded 1.02 g (74%) of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06297375B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-38fccca7a56d478895a5615cd8e105d4
출처 메모uspto-grants-2001_10