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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713412Generated: November 2, 2026

Butanoic acid, 2-[(3-nitrophenyl)methylene]-3-oxo-, 1-methylethyl ester → Azelnidipine

https://huagongshe.com/reaction/1713412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 2-[(3-nitrophenyl)methylene]-3-oxo-, 1-methylethyl esterHCID 3951175—
ReactantSodium MethoxideHCID 10942334—
Reactant1-Benzhydrylazetidin-3-YL 3-amino-3-iminopropanoate acetateHCID 45358292—
SolventIsopropanolHCID 3776—
ProductAzelnidipineHCID 6594888.2%

Reaction Steps

According to Japanese Examined Patent Publication (Kokoku) No. Hei 3-31715, sodium methoxide (0.27 g) was added to a solution of 2-(3-nitrobenzylidene)acetoacetic acid isopropyl ester (1.39 g) and amidinoacetic acid (1-benzhydryl-3-azetidinyl) ester acetate (1.62 g) in isopropyl alcohol (80 ml) and the mixture was heated under reflux for 4 hours. After the reaction mixture was cooled, insoluble material was removed and the solvent was evaporated under reduced pressure. The thus obtained residue was dissolved in ethyl acetate and the mixture was washed with water, followed by drying over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was subjected to silica gel column chromatography (toluene:ethyl acetate=3:1) to obtain pale yellow (±)-2-amino-1,4-dihydro-6-methyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 3-(1-diphenylmethylazetidin-3-yl) ester 5-isopropyl ester (2.17 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795281B2
Source datasetuspto-grants-2010_09
ORD IDord-4f45a28a2d2a4a0c87ad9c6b8c2cd641
Source noteuspto-grants-2010_09