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HRID 1073252作成日:2026年10月25日

Ethanol → 3-Amino-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acid

https://huagongshe.com/reaction/1073252

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物IsatinHCID 7054—
反応物Sodium HydroxideHCID 14798—
反応物2-Amino-1-((1,1'-biphenyl)-4-yl)ethan-1-one hydrochlorideHCID 12487182—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-Amino-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acidHCID 15085946—

反応条件

温度90 °C

反応手順

A 4.42 g portion of isatin was suspended in 25 ml of water in a three-necked 1 liter flask equipped with a reflux condenser and addition funnel. To this suspension was added a solution of 6.4 g of sodium hydroxide in 20 ml of water, then the mixture was heated to 90° C. A solution of 15.0 g of 2-amino-4'-phenylacetophenone, hydrochloride in 300 ml of a 50:50 mixture of ethanol:water was warmed slightly, then 100 ml of tetrahydrofuran was added to effect dissolution. This solution was added dropwise to the hot solution of isatin over 1.5 hours with vigorous stirring. When addition was complete, the solution was stirred at 90° C. for 1 hour and then the organic solvents were removed by distillation at 85° C. The remaining solution was cooled, filtered and the filtrate acidified to pH 5 with glacial acetic acid. The resulting solid was collected, washed with water and dried. The yellow solids were suspended in 40 ml of ethanol, filtered and dried, giving 2.19 g of the desired product, mp 223°-225° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04968702
出典データセットuspto-grants-1990_11
ORD IDord-208b9e45d46c47eab15f040892b6d5ef
出典メモuspto-grants-1990_11