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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248269Generated: October 27, 2026

Dimethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate → Dimethyl 4-[2-[4-(3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/2248269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 14306630—
SolventDimethylformamideHCID 6228—
ProductDimethyl 4-[2-[4-(3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 14306631183.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

In 20 ml of N,N-dimethylformamide was dissolved 1 g of dimethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. The solution was heated at 100° C. for 1.5 hours. The reaction solution was carefully poured onto 500 ml of ice water. The precipated oily substance was extracted with ethyl acetate. After drying over anhydrous sodium sulfate, the solvent was removed by distillation under reduced pressure. The obtained residue was subjected to silica gel column chromatography and eluted by chlorform:methanol (96:4 v/v). The obtained crude crystals were recrystallized form ethanol to give 1.2 g of dimethyl 4-[2-[4-(3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. This compound has the following physicochemical properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039674
Source datasetuspto-grants-1991_08
ORD IDord-0d9e087e17b44ea791db895fcfcbf867
Source noteuspto-grants-1991_08