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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721893Generated: November 1, 2026

Hydrochloric Acid → HCID 70394800, compound

https://huagongshe.com/reaction/1721893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantHCID 10740240HCID 10740240—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 70394800HCID 70394800—

Reaction Steps

A mixture of 16.4 g of 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid methyl ester 3-chloropropyl ester and 16.6 g of 4-(p-fluorobenzoyl)-piperidine is kept for 1 hour under argon in a bath heated to 145°. After cooling, 100 ml of ethyl acetate and 50 ml of 2N hydrochloric acid are added and the mixture is stirred until the reaction mass has completely dissolved. The partly oily aqueous-acidic phase is adjusted to pH 10 with 50% potassium carbonate solution; methylene chloride is added and the whole is filtered with suction. The methylene chloride phase of the filtrate is separated off and concentrated by evaporation and the residue is dissolved in ethyl acetate; the solution is dried over sodium sulphate and filtered. Filtration is then carried out over 1 kg of silica gel Merck 9385 using a hexane/ethyl acetate/methanol mixture (4:2:0.5) as eluant. The 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid methyl ester 3-[4-(p-fluorobenzoyl)-piperidino]-propyl ester obtained after working up is converted by means of ethereal hydrogen chloride solution into the hydrochloride which, after recrystallisation from isopropanol, melts at 198°-205° with the evolution of gas.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853393
Source datasetuspto-grants-1989_08
ORD IDord-8c6c6d28caf548e28f2807a1b13ac1ff
Source noteuspto-grants-1989_08