참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 4-fluoro-2-methyl-1H-indol-5-ol | HCID 10352036 | — |
| 반응물 | 7-Benzyloxy-4-chloro-6-methoxy cinnoline | HCID 21991008 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7-Benzyloxy-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline | HCID 10137481 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06887874B2 |
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| 출처 데이터셋 | uspto-grants-2005_05 |
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| ORD ID | ord-63d8f4327bec437ea8c1b2a818934aa0 |
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| 출처 메모 | uspto-grants-2005_05 |
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