Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4584Generated: October 24, 2026

Ethanol → 2-(N-nicotinoylamino)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/en/reaction/4584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl 3-aminocrotonateHCID 643918—
Reactant2-(N-nicotinoylamino)ethyl 2-(3-nitrobenzylidene)acetylacetateHCID 53905640—
Product2-(N-nicotinoylamino)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylateHCID 2015126170%

Reaction Steps

25 g (0.07 moles) of 2-(N-nicotinoylamino)ethyl 2-(3-nitrobenzylidene)acetylacetate and 7.51 g (0.07 moles) of methyl 3-aminocrotonate are heated uner reflux in 70 ml of ethanol for 45 minute. The solution is the cooled to room temperature to obtain 2-(N-nicotinoylamino)ethyl 2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate as yellow crystals melting--after recrystallisation in ethanol--at 207°-209° C. The yield is 70% of the theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727066
Source datasetuspto-grants-1988_02
ORD IDord-b5c35d1e26be4d9da180372b4123f748
Source noteuspto-grants-1988_02