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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9449생성일: 2026년 10월 23일

4-Vinylpyridine → 1-(2-methylpropyl)-8-(2-pyridin-4-ylvinyl)-1H-imidazo[4,5-c]-quinolin-4-amine

https://huagongshe.com/ko/reaction/9449

반응식

참여 물질

역할이름HCID투입량
반응물4-VinylpyridineHCID 7502—
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물8-bromo-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 11174597—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물1-(2-methylpropyl)-8-(2-pyridin-4-ylvinyl)-1H-imidazo[4,5-c]-quinolin-4-amineHCID 6881877465.1%

반응 조건

온도100 °C

반응 단계

Nitrogen was bubbled through a solution of 8-bromo-1-(2-methylpropyl)-1H-imidazo[4,5-c]-quinolin-4-amine (3.0 g, 9.4 mmol), 4-vinylpyridine (2.0 mL, 19 mmol), triphenylphosphine (246 mg, 0.94 mmol), and triethylamine (2.7 mL, 19 mmol) in acetonitrile (50 mL) for 15 minutes. Palladium (II) acetate (105 mg, 0.47 mmol) was added, and the reaction was heated at 100° C. for three days. The solvent was removed under reduced pressure, and the residue was adjusted to pH 2 with the addition of concentrated hydrochloric acid. Water was added, and the mixture was filtered through a layer of CELITE filter aid. Aqueous sodium carbonate (2 N) was added to the filtrate to adjust the solution to pH 10. The solution was then extracted with dichloromethane, and the combined extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by flash column chromatography on silica gel (eluting with chloroform:CMA in a gradient from 95:5 to 80:20) to provide 2.1 g of 1-(2-methylpropyl)-8-(2-pyridin-4-ylvinyl)-1H-imidazo[4,5-c]-quinolin-4-amine as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091214B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-06dcb0dc9288479ba77db93b0ebf51a7
출처 메모uspto-grants-2006_08