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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868333Generated: October 31, 2026

Potassium Carbonate → N-[3-(6-methyl-3-pyridyl)acryloyl]-4-(4-diphenylmethyl-1-piperazinyl)butylamine

https://huagongshe.com/reaction/868333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPivaloyl chlorideHCID 62493—
Reactant1-(4-Aminobutyl)-4-(diphenylmethyl)piperazineHCID 13956993—
Reactant3-(6-Methyl-3-pyridyl)acrylic acidHCID 54140853—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-[3-(6-methyl-3-pyridyl)acryloyl]-4-(4-diphenylmethyl-1-piperazinyl)butylamineHCID 6593372.3%

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a suspension of 2.71 g of 3-(6-methyl-3-pyridyl)acrylic acid in 70 ml of dry tetrahydrofuran, a solution of 1.68 g of triethylamine in 5 ml of dry tetrahydrofuran is added at room temperature. The resulting solution is cooled to -5° C., and a solution of 2.0 g of pivaloyl chloride in 5 ml of dry tetrahydrofuran is added slowly. The mixture is stirred at the same temperature for 0.5 hour and cooled to -10° C., and a solution of 6.43 g of 4-(4-diphenylmethyl-1-piperazinyl)butylamine in 5 ml of dry tetrahydrofuran is added slowly. The mixture is stirred for 0.5 hour at between -10° C. and -5° C. and then at room temperature overnight. To the reaction mixture is added 50 ml of 10% aqueous potassium carbonate, and the resulting mixture is extracted with three 100-ml portions of ethyl acetate. The combined extracts are washed with water and dried over magnesium sulfate, and the solvent is distilled off. The residue is recrystallized from acetonitrile to give 5.63 g of the title compound, m.p. 129°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778796
Source datasetuspto-grants-1988_10
ORD IDord-a404f031ff374c6fb9af01ee832418c5
Source noteuspto-grants-1988_10