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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334566생성일: 2026년 10월 25일

Hexane → 8-Methyl-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/334566

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물1-(Trimethylsilyl)prop-1-yneHCID 80363—
반응물2-(Chloromethyl)-8-methylimidazo[1,2-a]pyridineHCID 3254999—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물8-Methyl-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridineHCID 66598448100%

반응 조건

온도-78 °C

반응 단계

To a solution of trimethyl(prop-1-ynyl)silane (259 mg, 2.31 mmol) in THF (7.5 mL) at −78° C. was added n-BuLi 2.5M in hexane (1.1 mL, 2.8 mmol). After 90 min at −78° C. 2-(chloromethyl)-8-methyl-imidazo[1,2-a]pyridine (500 mg, 2.8 mmol) in THF (5 mL) was added dropwise. The solution became blue-green at −78° C. The solution was stirred at −78° C. for an additional 1 h. The reaction was quenched with water and the solvent was removed under reduced pressure. The crude product was purified over silicagel chromatography (prepacked 25 g silicagel column, DCM/MeOH from 100/0 to 99/1 as eluent) to afford 590 mg of 8-methyl-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine (Yield: 100%) as an yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883826B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-2e6d72e0b3334e52a9cd353e1ac45238
출처 메모uspto-grants-2014_11