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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481032Generated: October 26, 2026

2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- → Amlodipine 2-Phthalimide

https://huagongshe.com/reaction/481032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
ReactantEthyl 2-(2-chlorobenzylidene)-4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoateHCID 53879087—
SolventIsopropanolHCID 3776—
ProductAmlodipine 2-PhthalimideHCID 11157139—

Reaction Conditions

Temperature15 °C

Reaction Steps

116.7 g of ethyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate was dissolved in 120 ml of 2-propanol at 80° C. 31.2 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 180 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 92 ml of glacial acetic acid. The solid was dissolved in 75 ml of ethanol at 80° C. The solution was cooled to 20° C. and the suspension was agitated for 2 h. The solid was filtered off, washed with 25 ml of ethanol. The wet product was recrystallized from 60 ml of ethyl acetate. Yield: 43.6 g (30%) of the product, purity (HPLC, IN) −98.4%; m.p. 142.5-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653481B2
Source datasetuspto-grants-2003_11
ORD IDord-9dcb67f1f76d4273bb6540893f97d15e
Source noteuspto-grants-2003_11