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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329880Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-(4-Benzhydryl-1-piperazinyl)ethyl methyl 4-(2,1,3-benzoxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate dihydrochloride

https://huagongshe.com/reaction/329880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl 3-aminocrotonateHCID 643918—
Edukt2,1,3-Benzoxadiazole-4-carbaldehydeHCID 10290873—
EduktButanoic acid, 3-oxo-, 2-[4-(diphenylmethyl)-1-piperazinyl]ethyl esterHCID 11740518—
LösungsmittelIsopropanolHCID 3776—
Produkt2-(4-Benzhydryl-1-piperazinyl)ethyl methyl 4-(2,1,3-benzoxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate dihydrochlorideHCID 1987125945%

Reaktionsschritte

A mixture of 2,1,3-benzoxadiazole-4-carbaldehyde, 2-(4-benzhydryl-1-piperazinyl)ethyl acetoacetate and methyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 and the product obtained was further treated with methanolic hydrogen chloride solution to give 2-(4-benzhydryl-1-piperazinyl)ethyl methyl 4-(2,1,3-benzoxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate dihydrochloride as light yellow crystals, m.p. 192°-198° C. Yield 45.0%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04892875
Quelldatensatzuspto-grants-1990_01
ORD IDord-04b4bc05d1684e898c30c0fa33f2650e
Quellennotizuspto-grants-1990_01