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HRID 276856作成日:2026年10月25日
4-Methoxybenzylamine → 4-(3-Bromo-phenylamino)-6-(4-methoxy-benzylamino)-[1,7]naphthyridine-3-carbonitrile
https://huagongshe.com/reaction/276856
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-Methoxybenzylamine | HCID 75452 | — |
| 反応物 | 4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrile | HCID 18548979 | — |
| 反応物 | Chloroform methanol | HCID 21584188 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(3-Bromo-phenylamino)-6-(4-methoxy-benzylamino)-[1,7]naphthyridine-3-carbonitrile | HCID 12969105 | 45% |
反応手順
To 1 g of 4-(3-bromo-phenylamino)-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 25 mL of absolute ethanol was added 2 ml of 4-methoxy-benzylamine. The reaction was refluxed for eight days, stripped of solvents, and passed through a plug of silica gel with 5% methanol/chloroform. Fractions containing product were pooled and further purified by flash chromatography on silica gel with a gradient of 1-2% methanol/chloroform to give 595 mg (45%) of 4-(3-bromo-phenylamino)-6-(4-methoxy-benzylamino)-[1.7]naphthyridine-3-carbonitrile, which was sufficiently pure for further transformations. The product was recrystallized by dissolving in a minimum amount of warm chloroform, diluting with ether, and then adding hexanes to give 195 mg: melting point 82-86° C. (decomposed); mass spectrum (m/e): M+H 460.2, 462.2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06355636B1 |
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| 出典データセット | uspto-grants-2002_03 |
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| ORD ID | ord-7c7ed2f1ce5f4d07a71854f73667b027 |
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| 出典メモ | uspto-grants-2002_03 |
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