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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2180123생성일: 2026년 10월 26일

Cesium carbonate → 7-Benzyloxy-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline

https://huagongshe.com/reaction/2180123

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-fluoro-2-methyl-1H-indol-5-olHCID 10352036—
반응물7-Benzyloxy-4-chloro-6-methoxy cinnolineHCID 21991008—
용매DimethylformamideHCID 6228—
생성물7-Benzyloxy-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnolineHCID 1013748139%

반응 조건

온도95 °C

반응 단계

A mixture of 7-benzyloxy-4-chloro-6-methoxy cinnoline (2 g, 6.66 mmol), (prepared as described for the starting material in Example 1), 4-fluoro-5-hydroxy-2-methylindole (1.32 g, 7.99 mmol), (prepared as described for the starting material in Example 1), and cesium carbonate (3.2 g, 9.98 mmol) in DMF (40 ml) was heated at 95° C. for 1.5 hours. 4-Fluoro-5-hydroxy-2-methylindole (82 mg, 0.5 mmol) and cesium carbonate (3.2 g, 9.98 mmol) were added. The mixture was stirred for 1.5 hours at 115° C. The mixture was cooled, the solid was filtered and the filtrate was evaporated under vacuum. The residue was purified by column chromatography, eluting with methylene chloride/ethyl acetate (90/10 followed by 80/20) followed by methylene chloride/ethyl acetate/methanol (80/18/2). The fractions containing the expected product were combined and evaporated and the residue was triturated with ether/pentane (1/1). The solid was filtered, washed with pentane and dried under vacuum to give 7-benzyloxy-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline (1.1 g, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06887874B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-63d8f4327bec437ea8c1b2a818934aa0
출처 메모uspto-grants-2005_05