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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975603Generated: November 2, 2026

Potassium Carbonate → 2-[{4-(1-Imidazolylmethyl)benzylideneamino}oxy]ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/1975603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylateHCID 3016888—
Reactant4-(1-Imidazolylmethyl)benzaldoximeHCID 86747592—
SolventAcetonitrileHCID 6342—
Product2-[{4-(1-Imidazolylmethyl)benzylideneamino}oxy]ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylateHCID 86747591—

Reaction Steps

##STR36## 301 mg (0.763 mM) of 2-chloroethyl methyl 1,4-dihydro2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate and 155 mg (0.763 mM) of 4-(1-imidazolylmethyl)benzaldoxime were dissolved in 5 ml of dried acetonitrile, and then to the solution 58 mg (0.42 mM) of anhydrous potassium carbonate was added. After the mixture was heated under reflux for 15 hours, acetonitrile was distilled away and dichloromethane was added to the residue. After washing with water, the residue was dried over anhydrous sodium sulfate and dichloromethane was distilled away, and then the crystals were recrystallized from methanol, whereby the captioned compound was obtained. The yield was 400 mg (94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286869
Source datasetuspto-grants-1994_02
ORD IDord-e7e4464e74fa4aa0ba877773174fb7e0
Source noteuspto-grants-1994_02