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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1946423생성일: 2026년 10월 27일

Lithium Hexamethyldisilazide → N-(1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)-2-methylbenzamide

https://huagongshe.com/reaction/1946423

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-(Bromomethyl)-1-fluoro-3-(trifluoromethyl)benzeneHCID 2737573—
반응물HCID 178424292HCID 178424292—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물N-(1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)-2-methylbenzamideHCID 59547859—

반응 단계

1.0 M lithium bis(trimethylsilyl)amide (100 μl, 0.1 mmol, Aldrich) was slowly added to a solution of 2-methyl-N-1H-pyrazol-3-ylbenzamide (for a preparation see Intermediate 46)(22 mg, 0.1 mmol) in THF (400 μl). The resulting solution was then transferred to a solution of 2-fluoro-6-(trifluoromethyl)benzyl bromide (26 mg, 0.1 mmol, Aldrich) in THF (200 μl) and stirred for 1 h under nitrogen at ambient temperature. The mixture was diluted with DMSO (0.6 ml) and purified by MDAP using a Sunfire C18 (Method D) column using Acetonitrile-Water with a TFA modifier. The solvent was removed under a stream of nitrogen to give the title compound (27 mg); LCMS (System 3) MH+=378, tRET=1.13 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399436B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-e1bd2aa9fd4f4ffb913c7bfc0a1a7f4c
출처 메모uspto-grants-2013_03