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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 976016생성일: 2026년 10월 24일

(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine → 1,4-Bis((2R,5S)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-pyrazinyl)-but-2-yne

https://huagongshe.com/ko/reaction/976016

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 736066—
반응물2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazineHCID 3800909—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1,4-Bis((2R,5S)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-pyrazinyl)-but-2-yneHCID 1145284177%

반응 조건

온도-78 °C

반응 단계

(2R)-(-)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine 2.76 g (15mmol) was dissolved in 100 ml dry THF and cooled to -78° C., then 9.5 ml of a 1.6M solution BuLi (15 mmol) was added dropwise with stirring. After 1 hour 0.92 g (7.5 mmol) of 1,4-dichloro-2,3-butyne was introduced slowly. TLC and gas chromatography (GC) of the reaction mixture 1 hour later showed substantial amounts of unreacted 2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine and the monoalkylated product. The reaction was allowed to continue overnight and reach ambient temperature gradually. THF was evaporated off under reduced pressure and the residue partitioned between ether and water. The water phase was extracted twice with ether, dried (MgSO4) and evaporated. Kugelrohr distillation of the reaction mixture to give 2.3g (77%) pure product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05610141
출처 데이터셋uspto-grants-1997_03
ORD IDord-06cb4186efa54d49b3169c4ce264d158
출처 메모uspto-grants-1997_03