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HRID 7474作成日:2026年10月24日

5-Amino-2-chloro-4-fluorophenol → 2-Chloro-4-fluoro-5-{[6-methoxy-7-(2-methoxyethoxy)cinnolin-4-yl]amino}phenol

https://huagongshe.com/ja/reaction/7474

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-2-chloro-4-fluorophenolHCID 158654—
反応物4-Chloro-6-methoxy-7-(2-methoxyethoxy)cinnolineHCID 10707048—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-4-fluoro-5-{[6-methoxy-7-(2-methoxyethoxy)cinnolin-4-yl]amino}phenolHCID 6326407—

反応条件

温度140 °C

反応手順

A solution of 4-chloro-6-methoxy-7-(2-methoxyethoxy)cinnoline (0.2 g, 0.74 mmol), (prepared as described for the starting material in Example 2), and 4-chloro-2-fluoro-5-hydroxyaniline (132 mg, 0.82 mmol), (prepared as described in EP 061741 A2), in DMF (2.5 ml) was heated at 140° C. for 45 minutes. The work up procedure was as described in Example 6 and gave 4-(4-chloro-2-fluoro-5-hydroxyanilino)-6-methoxy-7-(2-methoxyethoxy)cinnoline as the hydrochloride salt (yellow solid, 157 mg, 49%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087602B2
出典データセットuspto-grants-2006_08
ORD IDord-f87dd80313104b09ac6647d75d7b9c3f
出典メモuspto-grants-2006_08