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HRID 749060作成日:2026年10月26日

Water → 4-(4-(2-Methoxyphenoxy)-anilino)-3-cyano-6-methoxy-7-(3-chloropropoxy)quinoline

https://huagongshe.com/reaction/749060

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物Potassium butoxideHCID 23699084—
反応物4-(4-(2-Methoxyphenoxy)-anilino)-3-cyano-6-methoxy-7-hydroxyquinolineHCID 135819831—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-(4-(2-Methoxyphenoxy)-anilino)-3-cyano-6-methoxy-7-(3-chloropropoxy)quinolineHCID 22048517—

反応手順

The product of step 2 (206.5 mg, 0.5 mmole) and 1-chloro-3-bromopropane (95 mg, 0.6 mmole) was dissolved in dimethylsulphoxide (5 ml) in the presence of potassium butoxide (0.55 ml, 11.0M in THF, 0.55 mmole) in and the mixture held at room temperature for 18 hours. Water was added and the mixture extracted with ethyl acetate. The combined extracts were washed with water and brine then dried (MgSO4) and evaporated to give 4-(4-(2-methoxyphenoxy)-anilino)-3-cyano-6-methoxy-7-(3-chloropropoxy)quinoline, intermediate 1, (189 mg, 77%) as a yellow gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07402583B2
出典データセットuspto-grants-2008_07
ORD IDord-d0286c75557a404eba88c05721252874
出典メモuspto-grants-2008_07