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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2211234Erstellt: 24. Oktober 2026

3-Nitrobenzaldehyde → 3-(1-Benzylpyrrolidin-3-yl) 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/de/reaction/2211234

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-NitrobenzaldehydeHCID 7449—
EduktMethyl 3-aminocrotonateHCID 643918—
Edukt1-Benzyl-3-acetoacetoxypyrrolidineHCID 13652812—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelChloroformHCID 6212—
Produkt3-(1-Benzylpyrrolidin-3-yl) 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylateHCID 229699,9%

Reaktionsschritte

In 5 ml of isopropanol were dissolved 1.51 g (0.01 mole) of 3-nitrobenzaldehyde, 2.61 g (0.01 mole) of 1-benzyl-3-acetoacetoxypyrrolidine, and 1.15 g (0.01 mole) of 3-aminocrotonic acid methyl ester and the solution thus obtained was refluxed for 8 hours. Then, the solvent was distilled off under reduced pressure, the residue thus formed was dissolved in chloroform, the solution was washed, in succession, with diluted hydrochloric acid, water, a saturated aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to provide 4.91 g of 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-(1-benzylpyrrolidin-3-yl)ester 5-methyl ester as a caramel form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05463064
Quelldatensatzuspto-grants-1995_10
ORD IDord-c2bd1187a86e4a06b74c5a2f9107eb03
Quellennotizuspto-grants-1995_10