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HRID 387691作成日:2026年10月25日

4-Nitrophenol → 7-Benzyloxy-6-cyano-4-(4-nitrophenoxy)quinoline

https://huagongshe.com/reaction/387691

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物2,6-LutidineHCID 7937—
反応物Carbonic acid--water (1/1)HCID 21993411—
反応物7-Benzyloxy-4-chloro-6-cyanoquinolineHCID 22646519—
溶媒TetrahydrofuranHCID 8028—
生成物7-Benzyloxy-6-cyano-4-(4-nitrophenoxy)quinolineHCID 2293659052.6%

反応条件

温度156.5 °C

反応手順

To the 7-benzyloxy-4-chloro-6-cyanoquinoline (2.60 g, 8.83 mmol) described in WO98/13350 there were added 4-nitrophenol (2.46 g, 17.7 mmol) and lutidine (2.06 ml, 17.7 mmol), and the mixture was heated and stirred at 155-158° C. for 2 hours. After returning the reaction system to room temperature, it was dissolved in tetrahydrofuran, saturated bicarbonate water was added and stirred therewith for 10 minutes, the mixture was concentrated under reduced pressure, the precipitated solid was filtered out and subjected to silica gel column chromatography (Fuji Silicia NH Type, eluent-hexane:ethyl acetate=50:50→ethyl acetate alone), the fraction containing the target substance was concentrated and the obtained solid was washed with diethyl ether. It was then dried under reduced pressure to obtain the title compound (1.84 g, 4.63 mmol, 52.6%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372981B2
出典データセットuspto-grants-2013_02
ORD IDord-c6a896a0302543df9d2f93bca11e601d
出典メモuspto-grants-2013_02