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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743034Generated: October 26, 2026

Triethylamine → 1-[(E)-3-Phenyl-3-(4-pyridyl)acryloyl]-4-(3,4,5-trimethoxybenzoyl)piperazine

https://huagongshe.com/reaction/743034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(3,4,5-Trimethoxybenzoyl)piperazineHCID 2874204—
ReactantHCID 67731480HCID 67731480—
SolventDichloromethaneHCID 6344—
Product1-[(E)-3-Phenyl-3-(4-pyridyl)acryloyl]-4-(3,4,5-trimethoxybenzoyl)piperazineHCID 1523054086.4%

Reaction Steps

1 ml of a methylene chloride solution containing 0.330 g of diphenylphosphoryl azide and then 0.280 g of 1-(3,4,5-trimethoxybenzoyl)piperazine were added to 5 ml of a methylene chloride solution containing both 0.224 g of (E)-3-phenyl-3-(4-pyridyl)acrylic acid (prepared as described in Preparation 3) and 0.28 ml of triethylamine. The mixture was then stirred for 4 hours at room temperature, after which the reaction solution was diluted with 20 ml of methylene chloride. It was then washed with a 5% w/v aqueous solution of sodium bicarbonate, followed by a saturated aqueous solution of sodium chloride, and the organic phase was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the oily residue (0.686 g) was purified by silica gel flash chromatography. 0.419 g of the title compound was obtained as a white powder from the fractions eluted with mixtures of methylene chloride and methanol ranging from 100:2 to 100:3 by volume.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556852
Source datasetuspto-grants-1996_09
ORD IDord-be8b3d5bc6f1449ba5b6bab0281d4c08
Source noteuspto-grants-1996_09