돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1822849생성일: 2026년 10월 24일

Acetic Acid → 4-[2-(Aminocarbonyl)anilino]-6,7-dimethoxy-3-quinolinecarboxamide

https://huagongshe.com/ko/reaction/1822849

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AnthranilamideHCID 6942—
반응물4-Chloro-6,7-dimethoxyquinoline-3-carboxamideHCID 22170204—
용매DimethylformamideHCID 6228—
생성물4-[2-(Aminocarbonyl)anilino]-6,7-dimethoxy-3-quinolinecarboxamideHCID 2217026641.7%

반응 조건

온도100 °C

반응 단계

A mixture of 4-chloro-6,7-dimethoxy-3-quinolinecarboxamide (0.046 g, 0.17 mmol), 2-aminobenzamide (0.029 g, 0.21 mmol) and acetic acid (40 μl) in DMF (0.8 ml) was heated at 100° C. for 6 h. After cooling the reaction mixture was evaporated. The residue was dissolved in a mixture of MeCN and water (1:3) containing 0.1% trifluoroacetic acid and the turbid solution was filtered through a plug of glass wool. Preparative HPLC using a gradient (containing 0.1% trifluoroacetic acid) of 10→40% MeCN in water as eluent gave, after evaporation, the title compound as the trifluoroacetic acid salt. The product was suspended in saturated aqueous NaHCO3 an absorbed on a short SPE column [ISOLUTE™ C18 (EC)] pre-conditioned subsequently with methanol and then water. The column was washed extensively with water until the pH of the eluent was neutral. The product was then eluted with methanol. After evaporation, the residue was crystallized from ethanol to give the title compound (26 mg, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07037925B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-de1bf3d214084f2aa382fa73e4cc257b
출처 메모uspto-grants-2006_05