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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1988071Erstellt: 25. Oktober 2026

Diethyl N-(4-aminobenzoyl)-L-glutamate → 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester

https://huagongshe.com/reaction/1988071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl N-(4-aminobenzoyl)-L-glutamateHCID 73002—
Edukt2-ChloropyrimidineHCID 74404—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl esterHCID 6733420769,4%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

2-Chloropyrimidine (0.72 g, 6.3 mmol) and N-(4-aminobenzoyl)-L-glutamic acid diethyl ester (2.04 g, 6.3 mmol, 1 equiv.) were dissolved in DMF (4 mL) and the resulting mixture was heated to 110° C. for 3 hrs. Reaction was complete as determined by TLC. The mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated by rotavap. The residue was purified by column chromatography (silica gel, 50% EtOAc/hexane) to afford 1.75 g of desired product 2-[4-(pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester in 69% yield. MS (ESI) m/z 399.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07553873B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-4842c3e460254e08a16f558392042157
Quellennotizuspto-grants-2009_06