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HRID 7470作成日:2026年10月24日

5-Amino-2-chloro-4-fluorophenol → 7-Benzyloxy-4-(4-chloro-2-fluoro-5-hydroxyanilino)-6-methoxycinnoline

https://huagongshe.com/ja/reaction/7470

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7-Benzyloxy-4-chloro-6-methoxycinnoline hydrochlorideHCID 21991007—
溶媒DimethylformamideHCID 6228—
生成物7-Benzyloxy-4-(4-chloro-2-fluoro-5-hydroxyanilino)-6-methoxycinnolineHCID 21991047—

反応手順

A solution of 7-benzyloxy-4-chloro-6-methoxycinnoline hydrochloride (3.4 g, 10 mmol) and 4-chloro-2-fluoro-5-hydroxyaniline, (prepared as described in EP 061741 A2), (1.84 g, 11 mmol) in DMF (42 ml) was heated at 130° C. for 20 minutes. The resulting solid was filtered off, washed with isopropanol, ether and dried under vacuum to give 7-benzyloxy-4-(4-chloro-2-fluoro-5-hydroxyanilino)-6-methoxycinnoline as the hydrochloride salt (yellow solid. 3.5 g, 75%).

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-62d71bbbedcf4e048364ce7e5a1dabe2
出典メモuspto-grants-2006_08