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HRID 1837363作成日:2026年10月27日
2-Methoxyethanol → 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-6-methoxy-7-(2-methoxyethoxy)quinoline-3-carbonitrile
https://huagongshe.com/reaction/1837363
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Methoxyethanol | HCID 8019 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-7-fluoro-6-methoxy-3-quinolinecarbonitrile | HCID 11486153 | — |
| 生成物 | 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-6-methoxy-7-(2-methoxyethoxy)quinoline-3-carbonitrile | HCID 5330110 | — |
反応手順
A mixture of sodium (118 mg, 5.11 mmol) and 2-methoxyethanol (5 mL) is heated at 120-130° C. for 3 hours. 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-7-fluoro-6-methoxy-3-quinolinecarbonitrile (500 mg, 1.28 mmol) is added and the reaction mixture is heated at 120-125° C. for 1 hour. The temperature of the reaction mixture is increased to 140-150° C. and this temperature is maintained for 2.5 hours. The reaction mixture is cooled to room temperature and diluted with ice cold aqueous sodium bicarbonate. The solid is collected by filtration washing with water and hexane. Purification by flash column chromatography, eluting with 2% methanol in dichloromethane provides 550 mg of 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-methoxy-7-[2-methoxyethoxy]-3-quinolinecarbonitrile, mp 210-212° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06780996B2 |
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| 出典データセット | uspto-grants-2004_08 |
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| ORD ID | ord-af770a3ee36f4aa78aca38859b1212ac |
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| 出典メモ | uspto-grants-2004_08 |
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