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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877999생성일: 2026년 10월 26일

3,5-Bis(trifluoromethyl)benzoyl chloride → N-(4-bromo-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide

https://huagongshe.com/reaction/877999

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물4-bromo-N-methylpyridin-3-amineHCID 68003905—
용매TetrahydrofuranHCID 8028—
생성물N-(4-bromo-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamideHCID 86670692—

반응 조건

온도-78 °C

반응 단계

To a solution of (4-bromo-pyridin-3-yl)-methyl-amine (1 g, 5.376 mmol) in THF (8 mL) was added LiHMDS (1M solution in THF, 10.7 mL, 10.7 mmol, CAS RN 4039-32-1) dropwise at −78° C., and stirred for 15 minutes before 3,5-bis-trifluoromethyl-benzoyl chloride (1.5 mL, 8.06 mmol, CAS RN 785-56-8) was added to the reaction mixture. After stirring at −78° C. for 1 h the reaction mixture was quenched with saturated aqueous NH4Cl solution (10 mL) and diluted with EtOAc (40 mL). The combined organic layers were washed with brine (15 mL), dried over anhydrous Na2SO4, filtered, and evaporated off in vacuo. The residue was purified by column chromatography over silica gel (15% EtOAc in n-hexane) to afford the title compound. Pale yellow solid (985 mg, 43%). MS (ESI): m/z=427.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987307B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-c62f8483bb5a462889152995cac312b1
출처 메모uspto-grants-2015_03