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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132829생성일: 2026년 10월 25일

(2S)-2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazine → (2R,5S)-2,5-dihydro-3,6-dimethoxy-2-(2'-fluoro-4'-(trifluoromethyl)benzyl)-5-isopropylpyrazine

https://huagongshe.com/reaction/132829

반응식

참여 물질

역할이름HCID투입량
반응물(2S)-2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazineHCID 736065—
반응물2-Fluoro-4-(trifluoromethyl)benzyl bromideHCID 2737570—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(2R,5S)-2,5-dihydro-3,6-dimethoxy-2-(2'-fluoro-4'-(trifluoromethyl)benzyl)-5-isopropylpyrazineHCID 20628238—

반응 단계

To a solution of 3.32 g (18 mmol) of commercially available (2S)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine in 100 mL of tetrahydrofuran at −70° C. was added 12 mL (19 mmol) of a 1.6M solution of butyllithium in hexanes. After stirring at this temperature for 20 min, 5 g (19.5 mmol) of 2-fluoro-4-trifluoromethylbenzyl bromide in 20 mL of tetrahydrofuran was added and stirring was continued for 3 h before warming the reaction to ambient temperature. The reaction was quenched with water, concentrated in vacuo, and extracted with ethyl acetate. The combined organic phase was washed with brine, dried, and concentrated in vacuo. Purification by flash chromatography (silica gel, 0-5% ethyl acetate in hexanes) afforded 5.5 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388019B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-9cbe7d45b5644e8b8f842d82f39779f5
출처 메모uspto-grants-2008_06