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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211234Generated: October 26, 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/reaction/2211234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantMethyl 3-aminocrotonateHCID 643918—
Reactant1-Benzyl-3-acetoacetoxypyrrolidineHCID 13652812—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
Product3-(1-Benzylpyrrolidin-3-yl) 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylateHCID 229699.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463064
Source datasetuspto-grants-1995_10
ORD IDord-c2bd1187a86e4a06b74c5a2f9107eb03
Source noteuspto-grants-1995_10