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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621537Generated: October 27, 2026

Ammonia → 3-cyclopropylmethyl 5-[2-(N-benzyl-N-methylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/621537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-[Methyl(phenylmethyl)amino]ethyl 3-oxobutanoateHCID 11776829—
ReactantCyclopropylmethyl 2-(3-nitrobenzylidene)acetoacetateHCID 53956239—
SolventEthanolHCID 702—
Product3-cyclopropylmethyl 5-[2-(N-benzyl-N-methylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylateHCID 306591442.1%

Reaction Steps

A mixture of 4.0 g (16 mmol) of 2-(N-benzyl-N-methylamino)ethyl acetoacetate, 4.6 g (16 mmol) of cyclopropylmethyl 2-(3-nitrobenzylidene)acetoacetate, 1.12 ml of 28% aqueous ammonia and 40 ml of ethanol was stirred at the reflux temperature for 8 hours, and then the solvent was removed under reduced pressure. The residue was chromatographed on silica gel column to afford 3-cyclopropylmethyl 5-[2-(N-benzyl-N-methylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate (3.5 g, 42.1%) as yellow oil. Treatment of this oil with hydrochloric acid gave the corresponding salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824855
Source datasetuspto-grants-1989_04
ORD IDord-54e3911edb1240338130292957529339
Source noteuspto-grants-1989_04