戻る
化工社化工社 化学情報印刷レポート · 研究参考用
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

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxybenzylamineHCID 75452—
反応物4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrileHCID 18548979—
反応物Chloroform methanolHCID 21584188—
溶媒EthanolHCID 702—
生成物4-(3-Bromo-phenylamino)-6-(4-methoxy-benzylamino)-[1,7]naphthyridine-3-carbonitrileHCID 1296910545%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355636B1
出典データセットuspto-grants-2002_03
ORD IDord-7c7ed2f1ce5f4d07a71854f73667b027
出典メモuspto-grants-2002_03