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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230374Erstellt: 24. Oktober 2026

Ethyl Acetate → HCID 57762568, Verbindung

https://huagongshe.com/de/reaction/230374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
Edukt(S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762562—
EduktHCID 57762606HCID 57762606—
KatalysatorTri-o-tolylphosphineHCID 80271—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 57762568HCID 5776256863,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Under an argon atmosphere, palladium acetate (19.9 mg) and tris(2-methylphenyl)phosphine (25.9 mg) were added to a suspension of (S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (514.4 mg), N-(4-iodophenyl)-N-isopropylpyrimidin-2-amine (577.4 mg) and potassium carbonate (352.9 mg) in DMF (6 ml), and the resulting mixture was stirred at 80° C. for 7 hours. After cooling the reaction solution to room temperature, ethyl acetate was added thereto, and the resulting mixture was washed twice with water and once with saturated brine, followed by drying the organic layers over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=2/1→1/1→1/3). The obtained crudely purified product was purified again by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=6/1-4/112/1) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (553.6 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566724B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-1a0084c7803f4e85906fb173dba7cfc5
Quellennotizuspto-grants-2009_07