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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280571Erstellt: 23. Oktober 2026

Amlodipine → 4-(2-Chlorophenyl)-3-ethoxycarbonyl-2-[2-(imidazolidin-2-on-1-ylcarbonylamino)ethoxymethyl]-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine

https://huagongshe.com/de/reaction/280571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmlodipineHCID 2162—
Edukt2-Oxoimidazolidine-1-carbonyl chlorideHCID 83241—
LösungsmittelChloroformHCID 6212—
LösungsmittelTriethylamineHCID 8471—
Produkt4-(2-Chlorophenyl)-3-ethoxycarbonyl-2-[2-(imidazolidin-2-on-1-ylcarbonylamino)ethoxymethyl]-5-methoxycarbonyl-6-methyl-1,4-dihydropyridineHCID 2332083455,4%

Reaktionsschritte

To a solution of 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine (1.0 g) in a mixture of chloroform (dried over alumina) (20 ml) and triethylamine (2 ml) was added imidazolidin-2-on-1-yl carbonyl chloride (0.36 g) in one portion and the mixture stirred at room temperature for 18 hours. After evaporation to dryness, the resultant oil was partitioned between 5% aqueous sodium carbonate and methylene chloride. The combined organic liquors were dried (MgSO4), filtered and evaporated to give 0.7 g of a yellow oil which crystallised from diisopropyl ether on standing to give pure title compound, (0.4 g), m.p. 145° C. Found: C, 54.94; H, 5.62; N, 10.62. C24H29ClN4O7 requires C, 55.33; H, 5.61; N, 10.76%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04590195
Quelldatensatzuspto-grants-1986_05
ORD IDord-8d6285e2a19844b09cd01ee36e7060af
Quellennotizuspto-grants-1986_05