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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543137Erstellt: 25. Oktober 2026

Amlodipine → 4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-[2-(3,4-dihydro-4-oxo-pyrimidin-2-ylamino)ethoxymethyl]-1,4-dihydropyridine

https://huagongshe.com/reaction/543137

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmlodipineHCID 2162—
Edukt2-(Methylthio)-1H-pyrimidin-4-oneHCID 79823—
LösungsmittelEthanolHCID 702—
Produkt4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-[2-(3,4-dihydro-4-oxo-pyrimidin-2-ylamino)ethoxymethyl]-1,4-dihydropyridineHCID 20199195—

Reaktionsschritte

2-[2-Aminoethoxymethyl]-3-ethoxycarbonyl-4-(2-chlorophenyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine (0.75 g) and 2-methylthio-3H-pyrimid-4-one (0.5 g) were dissolved in ethanol (5 ml) and heated under reflux for 20 hours. The solvent was evaporated and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with 2N hydrochloric acid to remove any unreacted amine, and then with dilute sodium hydroxide solution. It was then washed with water, dried, filtered and evaporated to give a yellow gum. Chromatography on silica "Kieselgel 60H" (Trade Mark) eluting with ethyl acetate gave the title compound, which was recrystallised from ethyl acetate, yield 171 mg, m.p. 148°-150°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04661485
Quelldatensatzuspto-grants-1987_04
ORD IDord-61848bf485f04a79bd5bb6ea400e164c
Quellennotizuspto-grants-1987_04