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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25479Generated: October 25, 2026

2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- → 3-Methyl 5-ethyl 4-(2-chlorophenyl)-2-{[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]methyl}-6-methyl-1,4-dihydro-3,5-pyridine dicarboxylate

https://huagongshe.com/reaction/25479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
ReactantMethyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—
SolventIsopropanolHCID 3776—
Product3-Methyl 5-ethyl 4-(2-chlorophenyl)-2-{[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]methyl}-6-methyl-1,4-dihydro-3,5-pyridine dicarboxylateHCID 11786009—

Reaction Conditions

Temperature15 °C

Reaction Steps

87 g of methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate was dissolved in 102 ml of 2-propanol at 80° C. 33.1 g of ethyl-3-aminocrotonate was added and the mixture was heated at the same temperature for 16 hours. The mixture was evaporated to dryness. The residue was dissolved in 153 ml of glacial acetic acid at 80° C. The mixture was cooled to 15° C. and stirred at the same temperature for 20 hours. The solid was filtered off and washed with 78 ml of glacial acetic acid. The solid was suspended in 150 ml of methanol and agitated at 60° C. for 30 minutes. The solid was cooled to 20° C. and filtered off, washed with 30 ml of methanol and dried. The product was recrystallized from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858738B2
Source datasetuspto-grants-2005_02
ORD IDord-249d482791444153aaceda86e7b6522a
Source noteuspto-grants-2005_02