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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230066Erstellt: 25. Oktober 2026

Triethylamine → 2-(Methoxycarbonyl)-5-nitrophenyl 4-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/230066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-MethylpiperazineHCID 53167—
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
EduktSalicylic acid, 4-nitro-, methyl esterHCID 139539—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Methoxycarbonyl)-5-nitrophenyl 4-methylpiperazine-1-carboxylateHCID 57632925—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a dry flask are added 2-hydroxy-4-nitro-benzoic acid methyl ester (40 mmol) (from Example 1h) and triphosgene (26.6 mmol) and DCM (100 mL). The reaction mixture is cooled to 0° C. and diisopropylethylamine (40 mmol) is added slowly. After addition the mixture is warmed to rt. After 1 h at this temperature it is refluxed for 1 h. The mixture is cooled down and the solvents are removed. THF (100 mL), Et3N (80 mmol), and N-methyl piperazine (80 mmol) are added and the mixture is stirred at rt overnight. The solvent is removed and the residue dissolved in EtOAc. Phases are separated upon addition of a 10% solution of NaHCO3. The organic phase is washed with brine, dried on Na2SO4 and evaporated. The crude is used in the following reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563894B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-ff89afc63ad34974acc5de0ac8fb91c3
Quellennotizuspto-grants-2009_07