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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5430생성일: 2026년 10월 24일

Sodium hydride → 5-[4-(Amino)butoxy]imidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/5430

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Amino-1-butanolHCID 25868—
반응물5-Chloroimidazo[1,2-A]pyridineHCID 10953722—
반응물Tert-butyldicarbonateHCID 22064466—
용매DimethylformamideHCID 6228—
생성물5-[4-(Amino)butoxy]imidazo[1,2-a]pyridineHCID 2336297941%

반응 단계

To a suspension of 60% sodium hydride (oily; 1.32 g, 33 mmloes) in DMF (60 ml) was added a solution of 5-chloroimidazo[1,2-a]pyridine (4.59 g, 30.1 mmoles) and 4-aminobutanol (2.68 g, 30.1 mmoles) in DMF (60 ml) at room temperature with stirring and the mixture was stirred at the same temperature for 5 hours. Tert-butyl dicarbonate (9.83 g, 45 mmoles) was added to the reaction solution, which was stirred at room temperature for 13 hours. After the solvent was distilled off, water was added to the residue, which was extracted with ether twice, washed with water and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was dissolved in methanol (20 ml), followed by the addition of conc. hydrochloric acid (20 ml) and stirring at room temperature for 1 hour. After the solvent was distilled off, chloroform was added to the residue, which was washed with 3N NaOH. After drying over anhydrous potassium carbonate, the solvent was distilled off. The residue was purified by column chromatography (eluent: methanol/chloroform=1:5) to obtain 2.53 g of the desired product (40.9%, light brown oily product).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244908
출처 데이터셋uspto-grants-1993_09
ORD IDord-0f285cb157234f1fa10f07e2d940a71c
출처 메모uspto-grants-1993_09