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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 387940Erstellt: 24. Oktober 2026

Cyclopropylamine → HCID 58930836, Verbindung

https://huagongshe.com/de/reaction/387940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopropylamineHCID 69828—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt1-(3-Diethylaminopropyl)-3-ethylcarbodiimide hydrochlorideHCID 9964512—
Edukt4-(4-(((4-Fluoroanilino)carbonyl)amino)phenoxy)-7-methoxy-6-quinolinecarboxylic acidHCID 22936350—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 58930836HCID 5893083644,5%

Reaktionsschritte

After dissolving the N-[4-(6-carboxy-7-methoxy-4-quinolyl)oxyphenyl]-N′-(4-fluorophenyl)urea (60 mg) synthesized in Example 341 in dimethylformamide (1.5 ml), there were added 1-ethyl-3-(3-diethylaminopropyl)-carbodiimide hydrochloride (39 mg), 1-hydroxy-1H-benzotriazole monohydrate (31 mg), triethylamine (30 μl) and cyclopropylamine (0.05 ml) and the mixture was stirred overnight at room temperature. The reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with water and then dried over anhydrous sodium sulfate. After distilling off the solvent, crystals were precipitated with ethyl acetate, filtered out and dried under reduced pressure to obtain the title compound (29 mg) as white crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08372981B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-3420ff75cd274140a16e1c02037ed533
Quellennotizuspto-grants-2013_02