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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butanoic acid, 2-[(3-nitrophenyl)methylene]-3-oxo-, 1-methylethyl ester | HCID 3951175 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Benzhydrylazetidin-3-YL 3-amino-3-iminopropanoate acetate | HCID 45358292 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Azelnidipine | HCID 65948 | 88.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795281B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-4f45a28a2d2a4a0c87ad9c6b8c2cd641 |
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| Source note | uspto-grants-2010_09 |
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