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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39697생성일: 2026년 10월 23일

Imidazole → 1-(1,3-dioxolan-2-ylmethyl)-7-(1H-imidazol-1-yl)-4-methylquinolin-2(1H)-one

https://huagongshe.com/ko/reaction/39697

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물7-Bromo-1-(1,3-dioxolan-2-ylmethyl)-4-methylquinolin-2(1h)-oneHCID 59398074—
촉매Copper oxideHCID 14829—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물1-(1,3-dioxolan-2-ylmethyl)-7-(1H-imidazol-1-yl)-4-methylquinolin-2(1H)-oneHCID 59397912—

반응 조건

온도142.5 °C

반응 단계

To 0.7 mL of an N,N-dimethylformamide solution containing 74 mg of 60% sodium hydride, 0.14 g of imidazole was added at room temperature, and the mixture was stirred for 10 minutes. Thereto were added 0.20 g of 7-bromo-1-(1,3-dioxolan-2-ylmethyl)-4-methylquinolin-2(1H)-one and 17 mg of copper(II) oxide, and the mixture was heated to 140 to 145° C. and stirred for 40 minutes. Thereto was further added 2 mL of N,N-dimethylformamide, and the mixture was further stirred for 1 hour. The reaction mixture was cooled to room temperature, then chloroform and water were added thereto, and the insoluble material filtered off. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=10:1] to obtain 77 mg of a brown oily substance, 1-(1,3-dioxolan-2-ylmethyl)-7-(1H-imidazol-1-yl)-4-methylquinolin-2(1H)-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-440530fd2e514d4ca5b600297af91348
출처 메모uspto-grants-2013_09