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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine | HCID 736066 | — |
| 반응물 | 2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazine | HCID 3800909 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,4-Bis((2R,5S)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-pyrazinyl)-but-2-yne | HCID 11452841 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05610141 |
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| 출처 데이터셋 | uspto-grants-1997_03 |
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| ORD ID | ord-06cb4186efa54d49b3169c4ce264d158 |
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| 출처 메모 | uspto-grants-1997_03 |
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