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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (2S)-2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazine | HCID 736065 | — |
| 반응물 | 2-Fluoro-4-(trifluoromethyl)benzyl bromide | HCID 2737570 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2R,5S)-2,5-dihydro-3,6-dimethoxy-2-(2'-fluoro-4'-(trifluoromethyl)benzyl)-5-isopropylpyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07388019B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-9cbe7d45b5644e8b8f842d82f39779f5 |
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| 출처 메모 | uspto-grants-2008_06 |
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