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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494258Erstellt: 25. Oktober 2026

7-Aminoquinoline → 9-Oxo-9H-fluorene-2-carboxylic acid quinolin-7-yl amide

https://huagongshe.com/reaction/494258

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7-AminoquinolineHCID 11377—
EduktFluorenone-2-carboxylic acidHCID 69913—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt9-Oxo-9H-fluorene-2-carboxylic acid quinolin-7-yl amideHCID 57682673—

Reaktionsschritte

To a solution of 7-aminoquinoline (D55) (35 mg, 0.24 mmol) in DCM (3 ml) was added 9-oxo-9H-fluorene-2-carboxylic acid (60 mg, 0.27 mmol), (3-dimethylamino-propyl)-ethyl-carbodiimide hydrochloride (68 mg, 0.36 mmol) and 4-dimethylaminopyridine (5 mg, 0.04 mmol) and the reaction stirred at room temperature then at reflux until complete by tlc. After cooling to room temperature the resultant precipitate was filtered off to give the title compound as an off-white solid. MS(ES): MH+ 351, M-H+ 349

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538121B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-e46a805cfcff40e3a1a945274cb69073
Quellennotizuspto-grants-2009_05