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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1073252Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1073252

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktIsatinHCID 7054—
EduktSodium HydroxideHCID 14798—
Edukt2-Amino-1-((1,1'-biphenyl)-4-yl)ethan-1-one hydrochlorideHCID 12487182—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Amino-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acidHCID 15085946—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04968702
Quelldatensatzuspto-grants-1990_11
ORD IDord-208b9e45d46c47eab15f040892b6d5ef
Quellennotizuspto-grants-1990_11