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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278088Erstellt: 26. Oktober 2026

Pyridine → Methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoate

https://huagongshe.com/reaction/278088

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktButyryl chlorideHCID 8855—
Edukt(E)-Methyl 4-(2-(dimethylamino)vinyl)-3-nitrobenzoateHCID 894337—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoateHCID 54551046—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a stirred mixture of methyl (E)-4-[2-(dimethylamino)vinyl]-3-nitrobenzoate (500 mg), which was prepared by the method of Brown et al. described in Journal of Medicinal Chemistry, vol. 35, page 2419 (1992), and pyridine (0.16 ml) in tetrahydrofuran (3 ml) was added butyryl chloride (0.21 ml) at 20° C. The reaction mixture was stirred at 40° C. for 24 hours and 50° C. for 4 hours. After cooled to 20° C., the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:1) to give methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoate (426 mg) as colorless amorphous.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358992B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-31ba064805a246c6b756045b3250a457
Quellennotizuspto-grants-2002_03