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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50191Erstellt: 24. Oktober 2026

Imidazolate → Methyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinate

https://huagongshe.com/de/reaction/50191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazolateHCID 3386966—
Edukt3-(4-Cyanophenyl)-propionic acidHCID 9361742—
EduktMethyl 5-amino-6-(methylamino)pyridine-3-carboxylateHCID 18412673—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinateHCID 18412623—

Reaktionsschritte

A solution of 2.6 g (15 mmol) of 3-(4-cyanophenyl)propionic acid in 25 mL of absolute tetrahydrofuran was mixed with 2.4 g (15 mmol) of N,N′-carbonyldiimidazole and stirred for 20 minutes at room temperature. Then the imidazolide was mixed with a solution of 2.3 g (13 mmol) of methyl 5-amino-6-methylaminonicotinate in 25 mL of dimethyfformamide and heated for 3 hours to 100° C. After the removal of the solvent in vacuo, the crude product obtained was taken up in ethyl acetate, the organic phase was washed with water and after drying over sodium sulfate it was again freed from solvent. The residue obtained was purified by flash chromatography (silica gel; gradient: dichloromethane to dichloromethane/ethanol=19:1). Yield: 2.1 g (50% of theory) of beige solid; Rf value: 0.54 (silica gel; ethyl acetate/ethanol/ammonia=90:10:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710055B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-8ed547a2fc2a4ce58ab475f72df20328
Quellennotizuspto-grants-2004_03