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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7070Erstellt: 23. Oktober 2026

Pentafluorophenol → N-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamide

https://huagongshe.com/de/reaction/7070

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentafluorophenolHCID 13041—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktN-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamideHCID 22019637—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamideHCID 2201959894,7%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A mixture of N-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamide (500 mg), pentafluorophenol (305 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (320 mg) and methylene chloride (10 ml) is stirred at 25° C. for 18 hours. The reaction solution is washed with water, and the solvent is evaporated under reduced pressure. To the residue are added ethyl acetate (10 ml) and cyclohexylamine (174 mg), and the mixture is heated with stirring at 60° C. for 18 hours. The solvent is evaporated and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (600 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084176B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-e923ca3883c74703a1879eb55299542a
Quellennotizuspto-grants-2006_08