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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1794371생성일: 2026년 10월 26일

2-Aminoquinoline → N-(2-quinolyl)-3-(5-phenyl-4-isoxazolyl)propionamide

https://huagongshe.com/reaction/1794371

반응식

참여 물질

역할이름HCID투입량
반응물2-AminoquinolineHCID 11379—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물3-(5-Phenyl-4-isoxazolyl)propionic acidHCID 22221254—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(2-quinolyl)-3-(5-phenyl-4-isoxazolyl)propionamideHCID 2222139284.1%

반응 단계

A mixture of 2-aminoquinoline (0.55 g), 3-(5-phenyl-4-isoxazolyl)propionic acid (0.82 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (0.68 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.91 g) and N,N-dimethylformamide (15 ml) was stirred at room temperature overnight. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate and then saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and N-(2-quinolyl)-3-(5-phenyl-4-isoxazolyl)propionamide (1.09 g, yield 84%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 112–113° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07022725B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-4360fc7ab4f94afba0107694c37084eb
출처 메모uspto-grants-2006_04